Category: 122775-35-3

Ethers do have nonbonding electron pairs on their oxygen atoms, 122775-35-3, formula is C8H11BO4, Name is 3,4-Dimethoxyphenylboronic acid. The ability to form hydrogen bonds with other compounds makes ethers particularly good solvents for a wide variety of organic compounds and a surprisingly large number of inorganic compounds. Quality Control of 122775-35-3.

Malamas, Michael S.;Pavlopoulos, Spiro;Alapafuja, Shakiru O.;Farah, Shrouq I.;Zvonok, Alexander;Mohammad, Khadijah A.;West, Jay;Perry, Nicholas Thomas;Pelekoudas, Dimitrios N.;Rajarshi, Girija;Shields, Christina;Chandrashekhar, Honrao;Wood, Jodi;Makriyannis, Alexandros research published 《 Design and Structure-Activity Relationships of Isothiocyanates as Potent and Selective N-Acylethanolamine-Hydrolyzing Acid Amidase Inhibitors》, the research content is summarized as follows. N-Acylethanolamines are signaling lipid mols. implicated in pathophysiol. conditions associated with inflammation and pain. N-Acylethanolamine acid amidase (NAAA) favorably hydrolyzes lipid palmitoylethanolamide, which plays a key role in the regulation of inflammatory and pain processes. The synthesis and structure-activity relationship studies encompassing the isothiocyanate pharmacophore have produced potent low nanomolar inhibitors for hNAAA, while exhibiting high selectivity (>100-fold) against other serine hydrolases and cysteine peptidases. We have followed a target-based structure-activity relationship approach, supported by computational methods and known cocrystals of hNAAA. We have identified systemically active inhibitors with good plasma stability (t_1/2 > 2 h) and microsomal stability (t_1/2 ∼ 15-30 min) as pharmacol. tools to investigate the role of NAAA in inflammation, pain, and drug addiction.

122775-35-3, 3,4-Dimethoxyphenylboronic acid is a useful research compound. Its molecular formula is C8H11BO4 and its molecular weight is 181.98 g/mol. The purity is usually 95%.
3,4-Dimethoxyphenylboronic acid contains varying amounts of anhydride.
3,4-Dimethoxyphenylboronic acid is a bacterial mutagen. A useful intermediate for organic synthesis.
3,4-Dimethoxyphenylboronic acid is a boronate ester that has been shown to be an effective coupling partner for the Suzuki reaction. It has also been used in cancer therapy and as a photochemical probe for the study of biological properties. 3,4-Dimethoxyphenylboronic acid has been shown to demethylate DNA and inhibit methionine aminopeptidase activity. It also cross-couples with halides, such as chlorides or iodides, and activates tertiary alcohols. 3,4-Dimethoxyphenylboronic acid is soluble in organic solvents and can be used in supramolecular chemistry., Quality Control of 122775-35-3

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Ethers feature bent C–O–C linkages. In dimethyl ether, the bond angle is 111° and C–O distances are 141 pm. 122775-35-3, formula is C8H11BO4, Name is 3,4-Dimethoxyphenylboronic acid. The barrier to rotation about the C–O bonds is low. The bonding of oxygen in ethers, alcohols, and water is similar. In the language of valence bond theory, the hybridization at oxygen is sp3. COA of Formula: C8H11BO4.

Manjappa, Kiran B.;Jhang, Jia-Wei;Lakshmi, K. C. Seetha;Yang, Ding-Yah research published 《 Four-Component Construction of Coumarin-Fused Pyrrolo[2,1-a]isoquinoline: Expedient Synthesis of Lamellarins and Their Regioselective Demethylation》, the research content is summarized as follows. Construction of the coumarin-fused pyrrolo[2,1-a]isolquinoline skeletons I (R = H, Me; R¹ = H, OMe; R² = H, OMe; R³ = H, OMe, Cl, diethylaminyl; R⁴ = H, Me; R⁵ = H; R⁴R⁵ = -(CH=CH-CH=CH)-; R⁶ = H) was realized through a four-component reaction between isoquinolines II, Et bromoacetate, o-hydroxybenzaldehydes 2-OH-4-R³-5-R⁴-6-R⁵C₆HCHO and nitromethane. This methodol. was further extended to the synthesis of lamellarin D tri-Me ether I (R = H; R¹ = R² = R³ = R⁴ = OMe; R⁵ = H; R⁶ = 3,4-dimethoxyphenyl) and a formal synthesis of lamellarin D. The controlled demethylation of lamellarin D tri-Me ether yielded dihydroxy and tetrahydroxy lamellarin analogs I (R = H; R¹ = R² = OMe; R³ = OH, OMe; R⁴ = OH, OMe; R⁵ = H; R⁶ = 3,4-dihydroxyphenyl, 3,4-dimethoxyphenyl) regioselectively.

122775-35-3, 3,4-Dimethoxyphenylboronic acid is a useful research compound. Its molecular formula is C8H11BO4 and its molecular weight is 181.98 g/mol. The purity is usually 95%.
3,4-Dimethoxyphenylboronic acid contains varying amounts of anhydride.
3,4-Dimethoxyphenylboronic acid is a bacterial mutagen. A useful intermediate for organic synthesis.
3,4-Dimethoxyphenylboronic acid is a boronate ester that has been shown to be an effective coupling partner for the Suzuki reaction. It has also been used in cancer therapy and as a photochemical probe for the study of biological properties. 3,4-Dimethoxyphenylboronic acid has been shown to demethylate DNA and inhibit methionine aminopeptidase activity. It also cross-couples with halides, such as chlorides or iodides, and activates tertiary alcohols. 3,4-Dimethoxyphenylboronic acid is soluble in organic solvents and can be used in supramolecular chemistry., COA of Formula: C8H11BO4

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Ethers can again be classified into two varieties: if the alkyl or aryl groups are the same on both sides of the oxygen atom, 122775-35-3, formula is C8H11BO4, Name is 3,4-Dimethoxyphenylboronic acid. Then it is a simple or symmetrical ether, whereas if they are different, the ethers are called mixed or unsymmetrical ethers. Formula: C8H11BO4.

Masson-Makdissi, Jeanne;Prieto, Liher;Abel-Snape, Xavier;Lautens, Mark research published 《 Enantio- and Diastereodivergent Sequential Catalysis Featuring Two Transition-Metal-Catalyzed Asymmetric Reactions》, the research content is summarized as follows. This study demonstrated the feasibility and inherent benefits of combining two distinct asym. transition-metal-catalyzed reactions in one pot. The reported transformation feature a Pd-catalyzed asym. allylic alkylation and a Rh-catalyzed enantioselective 1,4-conjugate addition, effectively converting simple allyl enol carbonate precursors into enantioenriched cyclic ketones such as I [R = Me, (CH₂)₂CN, (CH₂)₂CO₂Me, CH₂OTBS; Ar = C₆H₅, 2-MeC₆H₄, 2-naphthyl, etc.] with two remote stereocenters. Despite the anticipated challenges associated with controlling stereoselectivity in such a complex system, the products were obtained in enantiomeric excesses ranging up to >99% ee, exceeding those obtained from either of the individual asym. reactions. In addition, since the stereoselectivity of both steps was under catalyst control, this one-pot reaction was enantio- and diastereodivergent, enabling facile access to all stereoisomers from the same set of starting materials.

Formula: C8H11BO4, 3,4-Dimethoxyphenylboronic acid is a useful research compound. Its molecular formula is C8H11BO4 and its molecular weight is 181.98 g/mol. The purity is usually 95%.
3,4-Dimethoxyphenylboronic acid contains varying amounts of anhydride.
3,4-Dimethoxyphenylboronic acid is a bacterial mutagen. A useful intermediate for organic synthesis.
3,4-Dimethoxyphenylboronic acid is a boronate ester that has been shown to be an effective coupling partner for the Suzuki reaction. It has also been used in cancer therapy and as a photochemical probe for the study of biological properties. 3,4-Dimethoxyphenylboronic acid has been shown to demethylate DNA and inhibit methionine aminopeptidase activity. It also cross-couples with halides, such as chlorides or iodides, and activates tertiary alcohols. 3,4-Dimethoxyphenylboronic acid is soluble in organic solvents and can be used in supramolecular chemistry., 122775-35-3.

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Ethers do have nonbonding electron pairs on their oxygen atoms, 122775-35-3, formula is C8H11BO4, Name is 3,4-Dimethoxyphenylboronic acid. The ability to form hydrogen bonds with other compounds makes ethers particularly good solvents for a wide variety of organic compounds and a surprisingly large number of inorganic compounds. Name: 3,4-Dimethoxyphenylboronic acid.

Li, Zhe;Powers, Mitchell;Ivey, Kayla;Adas, Sonya;Ellman, Brett;Bunge, Scott D.;Twieg, Robert J. research published �Fluorinated triphenylenes and a path to short tailed discotic liquid crystals: synthesis, structure and transport properties� the research content is summarized as follows. A new synthetic approach for fluorinated alkoxytriphenylene discotic liquid crystals is presented. This methodol. exploits the previously described photocyclodehydrofluorination (PCDHF) reaction for the preparation of fluorinated triphenylene derivatives coupled with a variety of nucleophilic aromatic substitution (S_NAr) reactions. This particular combination of reactions provides a versatile route to discotic materials with carefully controlled core fluorine and alkoxy tail content. In the course of these studies, new discotic materials with minimal tail content have been revealed. The mesogenic properties of these materials are reported, and their charge transport properties are measured using the time of flight technique.

Name: 3,4-Dimethoxyphenylboronic acid, 3,4-Dimethoxyphenylboronic acid is a useful research compound. Its molecular formula is C8H11BO4 and its molecular weight is 181.98 g/mol. The purity is usually 95%.
3,4-Dimethoxyphenylboronic acid contains varying amounts of anhydride.
3,4-Dimethoxyphenylboronic acid is a bacterial mutagen. A useful intermediate for organic synthesis.
3,4-Dimethoxyphenylboronic acid is a boronate ester that has been shown to be an effective coupling partner for the Suzuki reaction. It has also been used in cancer therapy and as a photochemical probe for the study of biological properties. 3,4-Dimethoxyphenylboronic acid has been shown to demethylate DNA and inhibit methionine aminopeptidase activity. It also cross-couples with halides, such as chlorides or iodides, and activates tertiary alcohols. 3,4-Dimethoxyphenylboronic acid is soluble in organic solvents and can be used in supramolecular chemistry., 122775-35-3.

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Ethers are a class of organic compounds that contain an ether group—an oxygen atom connected to two alkyl or aryl groups. 122775-35-3, formula is C8H11BO4, Name is 3,4-Dimethoxyphenylboronic acid.They have the general formula R–O–Râ€? where R and Râ€?represent the alkyl or aryl groups. Reference of 122775-35-3.

Liljenberg, Sara;Nain-Perez, Amalyn;Nilsson, Oscar;Matic, Josipa;Groetli, Morten research published �Environmentally friendly catechol-based synthesis of dibenzosultams� the research content is summarized as follows. An environmentally friendly route of synthesis is reported for sultams containing a catechol function in the secondary aromatic ring (ring B), e.g., I making use of water as a solvent. The reaction can also be paired with THF for enhanced solubility It occurs by the application of a base and heat and proceeds through what is presumably an oxidation of the catechol function followed by nucleophilic addition by the nitrogen of the sulfonamide. The reaction is robust and reproducible, as demonstrated by the successful synthesis of eight different sultams with significant variation possible in both the primary aromatic ring (ring A) and in the group attached to the sultam nitrogen, with isolated yields of 43-86% after purification

122775-35-3, 3,4-Dimethoxyphenylboronic acid is a useful research compound. Its molecular formula is C8H11BO4 and its molecular weight is 181.98 g/mol. The purity is usually 95%.
3,4-Dimethoxyphenylboronic acid contains varying amounts of anhydride.
3,4-Dimethoxyphenylboronic acid is a bacterial mutagen. A useful intermediate for organic synthesis.
3,4-Dimethoxyphenylboronic acid is a boronate ester that has been shown to be an effective coupling partner for the Suzuki reaction. It has also been used in cancer therapy and as a photochemical probe for the study of biological properties. 3,4-Dimethoxyphenylboronic acid has been shown to demethylate DNA and inhibit methionine aminopeptidase activity. It also cross-couples with halides, such as chlorides or iodides, and activates tertiary alcohols. 3,4-Dimethoxyphenylboronic acid is soluble in organic solvents and can be used in supramolecular chemistry., Reference of 122775-35-3

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Ethers can again be classified into two varieties: if the alkyl or aryl groups are the same on both sides of the oxygen atom, 122775-35-3, formula is C8H11BO4, Name is 3,4-Dimethoxyphenylboronic acid. Then it is a simple or symmetrical ether, whereas if they are different, the ethers are called mixed or unsymmetrical ethers. Category: ethers-buliding-blocks.

Lin, Shibo;Liang, Yuru;Cheng, Jiayi;Pan, Feng;Wang, Yang research published ã€?Novel diaryl-2H-azirines: Antitumor hybrids for dual-targeting tubulin and DNAã€? the research content is summarized as follows. A novel class of diaryl substituted 2H-azirines I [R = H, 4-Me, 3,4,5-tri-MeO, etc., R¹ = H, 4-Me, 4-EtO, etc.] were designed based on combination of pharmacophores from Combretastatin A-4 (CA-4) and aziridine-type alkylating agents, which are known tubulin polymerization inhibitor and DNA damaging agents, resp. The antitumor activities of these compounds I were evaluated in-vitro and compound I [R = 3-F-4-MeO, R¹ =3,4,5-tri-MeO] showed the most potent activities against four cancer cell lines with IC₅₀ values ranging from 0.16 to 1.40μM. Further mechanistic studies revealed that compound I [R = 3-F-4-MeO, R¹ =3,4,5-tri-MeO] worked as a bifunctional agent targeting both tubulin and DNA. In the nude mice xenograft model, compound I [R = 3-F-4-MeO, R¹ =3,4,5-tri-MeO] significantly inhibited the tumor growth with low toxicity, demonstrating the promising potential for further developing novel cancer therapy with a unique mechanism.

Category: ethers-buliding-blocks, 3,4-Dimethoxyphenylboronic acid is a useful research compound. Its molecular formula is C8H11BO4 and its molecular weight is 181.98 g/mol. The purity is usually 95%.
3,4-Dimethoxyphenylboronic acid contains varying amounts of anhydride.
3,4-Dimethoxyphenylboronic acid is a bacterial mutagen. A useful intermediate for organic synthesis.
3,4-Dimethoxyphenylboronic acid is a boronate ester that has been shown to be an effective coupling partner for the Suzuki reaction. It has also been used in cancer therapy and as a photochemical probe for the study of biological properties. 3,4-Dimethoxyphenylboronic acid has been shown to demethylate DNA and inhibit methionine aminopeptidase activity. It also cross-couples with halides, such as chlorides or iodides, and activates tertiary alcohols. 3,4-Dimethoxyphenylboronic acid is soluble in organic solvents and can be used in supramolecular chemistry., 122775-35-3.

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Ethers feature bent C–O–C linkages. In dimethyl ether, the bond angle is 111° and C–O distances are 141 pm. 122775-35-3, formula is C8H11BO4, Name is 3,4-Dimethoxyphenylboronic acid. The barrier to rotation about the C–O bonds is low. The bonding of oxygen in ethers, alcohols, and water is similar. In the language of valence bond theory, the hybridization at oxygen is sp3. SDS of cas: 122775-35-3.

Liu, Wenchao;Chen, Huan;Zhang, Xiaonan;Zhang, Xin;Xu, Long;Lei, Yanqi;Zhu, Changjin;Ma, Bing research published ã€?Isatin derivatives as a new class of aldose reductase inhibitors with antioxidant activityã€? the research content is summarized as follows. In this work, isatin was employed as the scaffold to design aldose reductase inhibitors with antioxidant activity. Most of the isatin derivatives were proved to be excellent in the inhibition of aldose reductase (ALR2) with IC50 values at submicromolar level, and (E)-2-(5-(4-methoxystyryl)-2,3-dioxoindolin-1-yl) acetic acid (9g) was identified as the most effective with an IC50 value of 0.015 μM. Moreover, compounds 9a-h with styryl side chains at the C5 position of isatin showed potent antioxidant activity. Particularly, the phenolic compound 9h demonstrated similar antioxidant activity with the well-known antioxidant Trolox. Structure-activity relationship and mol. docking studies showed that the acetic acid group at N1 and C5 p-hydroxystyryl side chain were the key structures to increase the aldose reductase inhibitory activity and antioxidant activity. [graphic not available: see fulltext]

122775-35-3, 3,4-Dimethoxyphenylboronic acid is a useful research compound. Its molecular formula is C8H11BO4 and its molecular weight is 181.98 g/mol. The purity is usually 95%.
3,4-Dimethoxyphenylboronic acid contains varying amounts of anhydride.
3,4-Dimethoxyphenylboronic acid is a bacterial mutagen. A useful intermediate for organic synthesis.
3,4-Dimethoxyphenylboronic acid is a boronate ester that has been shown to be an effective coupling partner for the Suzuki reaction. It has also been used in cancer therapy and as a photochemical probe for the study of biological properties. 3,4-Dimethoxyphenylboronic acid has been shown to demethylate DNA and inhibit methionine aminopeptidase activity. It also cross-couples with halides, such as chlorides or iodides, and activates tertiary alcohols. 3,4-Dimethoxyphenylboronic acid is soluble in organic solvents and can be used in supramolecular chemistry., SDS of cas: 122775-35-3

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Ethers are a class of organic compounds that contain an ether group—an oxygen atom connected to two alkyl or aryl groups. 122775-35-3, formula is C8H11BO4, Name is 3,4-Dimethoxyphenylboronic acid.They have the general formula R–O–Râ€? where R and Râ€?represent the alkyl or aryl groups. Related Products of 122775-35-3.

Luo, Na;Fang, Xiaoyu;Su, Mingbo;Zhang, Xinwen;Li, Dan;Li, Honglin;Li, Shiliang;Zhao, Zhenjiang research published ã€?Design, Synthesis and SAR Studies of Novel and Potent Dipeptidyl Peptidase 4 Inhibitorsã€? the research content is summarized as follows. To discover novel and potent DPP-4 inhibitors, three series of compounds I [R = H, Br, MeO(O)C, etc.] , II, III [R¹ = Br, Ph, 2,4-difluorophenyl, etc.] and IV [R² = H, Br, MeO; R³ = H, Br, CN, HO(O)C] were designed and synthesized in this study based on previously identified novel scaffold of 2-phenyl-3,4-dihydro-2H-benzo[f]chromen-3-amine. Among the designed compounds, IV [R² = H, R³ = CN] was the most potent one with an IC₅₀ value of 16.00 nM. Besides, IV [R² = H, R³ = CN] (5 mg/kg) displayed a moderate glucose tolerance capability in ICR mice. Structure-activity-relationship (SAR) studies were discussed in detail, which was constructive for further optimization.

122775-35-3, 3,4-Dimethoxyphenylboronic acid is a useful research compound. Its molecular formula is C8H11BO4 and its molecular weight is 181.98 g/mol. The purity is usually 95%.
3,4-Dimethoxyphenylboronic acid contains varying amounts of anhydride.
3,4-Dimethoxyphenylboronic acid is a bacterial mutagen. A useful intermediate for organic synthesis.
3,4-Dimethoxyphenylboronic acid is a boronate ester that has been shown to be an effective coupling partner for the Suzuki reaction. It has also been used in cancer therapy and as a photochemical probe for the study of biological properties. 3,4-Dimethoxyphenylboronic acid has been shown to demethylate DNA and inhibit methionine aminopeptidase activity. It also cross-couples with halides, such as chlorides or iodides, and activates tertiary alcohols. 3,4-Dimethoxyphenylboronic acid is soluble in organic solvents and can be used in supramolecular chemistry., Related Products of 122775-35-3

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Ethers can again be classified into two varieties: if the alkyl or aryl groups are the same on both sides of the oxygen atom, 122775-35-3, formula is C8H11BO4, Name is 3,4-Dimethoxyphenylboronic acid. Then it is a simple or symmetrical ether, whereas if they are different, the ethers are called mixed or unsymmetrical ethers. Synthetic Route of 122775-35-3.

Li, Yang;Sun, Ning;Hao, Meng;Zhang, Cai-Lin;Li, Hong;Zhu, Wen-Qing research published ã€?Nanopalladium-Catalyzed Oxidative Heck Reaction of Fluorinated Olefins: H₂O₂ as a Green Oxidantã€? the research content is summarized as follows. Pd-based nanocatalysts were prepared through immobilization of Pd(OAc)₂/phenanthroline on nanocarbon materials and subsequent pyrolysis. The catalysts were characterized by X-ray diffraction (XRD), XPS and electron microscopy (TEM). Pd-based nanocatalysts can efficiently catalyze the oxidative Heck reaction of 2,3,3,3-tetrafuoroprop-1-ene by using H₂O₂ as a green oxidant and generate (Z)-β-fluoro-β-(trifluoromethyl)styrenes RCH=C(F)CF₃ (R = 4-methylphenyl, 3-methoxyphenyl, 2H-1,3-benzodioxol-5-yl, etc.) in excellent yield. The yield and Z/E selectivity of the titled reaction remained higher than 90% after four reaction cycles.

122775-35-3, 3,4-Dimethoxyphenylboronic acid is a useful research compound. Its molecular formula is C8H11BO4 and its molecular weight is 181.98 g/mol. The purity is usually 95%.
3,4-Dimethoxyphenylboronic acid contains varying amounts of anhydride.
3,4-Dimethoxyphenylboronic acid is a bacterial mutagen. A useful intermediate for organic synthesis.
3,4-Dimethoxyphenylboronic acid is a boronate ester that has been shown to be an effective coupling partner for the Suzuki reaction. It has also been used in cancer therapy and as a photochemical probe for the study of biological properties. 3,4-Dimethoxyphenylboronic acid has been shown to demethylate DNA and inhibit methionine aminopeptidase activity. It also cross-couples with halides, such as chlorides or iodides, and activates tertiary alcohols. 3,4-Dimethoxyphenylboronic acid is soluble in organic solvents and can be used in supramolecular chemistry., Synthetic Route of 122775-35-3

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Ethers feature bent C–O–C linkages. In dimethyl ether, the bond angle is 111° and C–O distances are 141 pm. 122775-35-3, formula is C8H11BO4, Name is 3,4-Dimethoxyphenylboronic acid. The barrier to rotation about the C–O bonds is low. The bonding of oxygen in ethers, alcohols, and water is similar. In the language of valence bond theory, the hybridization at oxygen is sp3. Related Products of 122775-35-3.

Li, Ya-Sheng;Mao, Shen;Zhao, Dong-Sheng;Wang, Can-Can;Zu, Dan;Yang, Xi;Liu, Gui-Jun;Wang, Si-Jia;Zhang, Bo;Bao, Xiao-Ze;Ye, Xin-Yi;Wei, Bin;Cui, Zi-Ning;Chen, Jian-Wei;Wang, Hong research published ã€?Rational design of phenyl thiophene (pyridine) derivatives that overcome P-glycoprotein mediated MDR in MCF-7/ADR cellã€? the research content is summarized as follows. Glycoprotein (P-gp)-mediated multidrug resistance (MDR) has become an important hindrance in the clin. treatment of malignant tumors. In this paper, based on our lead compound and strategies of bioisosteric replacement and alkoxy effect, phenylthiophene and phenylpyridine derivatives were designed as chemosensitizers for front-line antineoplastic agents and overcomes P-gp mediated MDR in MCF-7/ADR cell. Generally, 4-phenylthiophene-2-carboxamide derivative I has been screened and obtained with optimal activity against P-gp mediated MDR in MCF-7/ADR (IC₅₀ (doxorubicin) = 1.02μM, RF = 49.9 with 5μM 60 treated). The results of western blot and Rh123 accumulation assays showed that I effectively inhibited P-gp efflux function but not its expression. It is noted that compound I is a potentially broad-spectrum chemosensitizer in combination with commonly used anti-tumor drugs, such as doxorubicin, paclitaxel, daunorubicin and vincristine with RF value of 20-80.

Related Products of 122775-35-3, 3,4-Dimethoxyphenylboronic acid is a useful research compound. Its molecular formula is C8H11BO4 and its molecular weight is 181.98 g/mol. The purity is usually 95%.
3,4-Dimethoxyphenylboronic acid contains varying amounts of anhydride.
3,4-Dimethoxyphenylboronic acid is a bacterial mutagen. A useful intermediate for organic synthesis.
3,4-Dimethoxyphenylboronic acid is a boronate ester that has been shown to be an effective coupling partner for the Suzuki reaction. It has also been used in cancer therapy and as a photochemical probe for the study of biological properties. 3,4-Dimethoxyphenylboronic acid has been shown to demethylate DNA and inhibit methionine aminopeptidase activity. It also cross-couples with halides, such as chlorides or iodides, and activates tertiary alcohols. 3,4-Dimethoxyphenylboronic acid is soluble in organic solvents and can be used in supramolecular chemistry., 122775-35-3.

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem