Category: 103-16-2

A mild and practical method for deprotection of aryl methyl/benzyl/allyl ethers with HPPh₂ and ^tBuOK was written by Pan, Wenjing;Li, Chenchen;Zhu, Haoyin;Li, Fangfang;Li, Tao;Zhao, Wanxiang. And the article was included in Organic & Biomolecular Chemistry in 2021.Recommanded Product: 103-16-2 The following contents are mentioned in the article:

A general method for the demethylation, debenzylation, and deallylation of aryl ethers ROMe (R = C₆H₅, 3-FC₆H₄, 2-naphthyl, etc.), R¹OCH²Ph (R¹ = C₆H₅, 5,6,7,8-tetrahydronaphthalen-2-yl, 2-naphthyl, etc.) and R²OCH²CH=CH² (R² = C₆H₅, 2,3-dimethylphenyl, 1-naphthyl, etc.) using HPPh₂ and ^tBuOK is reported. The reaction features mild and metal-free reaction conditions, broad substrate scope, good functional group compatibility, and high chem. selectivity towards aryl ethers over aliphatic structures. Notably, this approach is competent to selectively deprotect the allyl or benzyl group, making it a general and practical method in organic synthesis. This study involved multiple reactions and reactants, such as 4-Benzyloxyphenol (cas: 103-16-2Recommanded Product: 103-16-2).

4-Benzyloxyphenol (cas: 103-16-2) belongs to ethers. Esters perform as high-grade solvents for a broad array of plastics, plasticizers, resins, and lacquers, and are one of the largest classes of synthetic lubricants on the commercial market. Polyesters are important plastics, with monomers linked by ester moieties. Liquid esters of low volatility serve as softening agents for resins and plastics. Esters also include many industrially important polymers. Polymethyl methacrylate is a glass substitute sold under the names Lucite and Plexiglas; polyethylene terephthalate is used as a film (Mylar) and as textile fibres sold as Terylene, Fortrel, and Dacron.Recommanded Product: 103-16-2

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

Synthesis of new substituted (2H-chromen-2-one)-phenol derivatives: An approach to molecular docking and antimicrobial assession was written by Mangasuli, Sumitra N.;Managutti, Praveen B.;Hosamani, Kallappa M.;Joshi, Shrinivas D.. And the article was included in Chemical Data Collections in 2020.Application of 103-16-2 The following contents are mentioned in the article:

A number of new substituted (2H-chromen-2-one)-phenol derivatives I [R = Me, Cl, Br, etc.] were synthesized by Williamson ether reaction follows an S_N² bimol. nucleophilic substitution mechanism. The titled compounds I was characterized by IR, ¹H NMR, ¹³C NMR and Mass spectral studies. As predicted, the derivatization of benzyloxy phenol with coumarin via ether linkage enhanced the activity of the titled compounds I against four bacterial and four fungal strains. Compound I [R = 1-naphthyloxy] showed significant strong anti-microbial broad spectrum activity against all tested bacterial and fungal strains. Anti-bacterial assay against standard coupled with in-silico mol. docking studies indicated that I [R = 1-naphthyloxy] showed promising activity with higher C-score values. This study involved multiple reactions and reactants, such as 4-Benzyloxyphenol (cas: 103-16-2Application of 103-16-2).

4-Benzyloxyphenol (cas: 103-16-2) belongs to ethers. Esters typically have a pleasant smell; those of low molecular weight are commonly used as fragrances and are found in essential oils and pheromones. Esterification is the general name for a chemical reaction in which two reactants (typically an alcohol and an acid) form an ester as the reaction product. Esters are common in organic chemistry and biological materials.Application of 103-16-2

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

Synthesis of new substituted (2H-chromen-2-one)-phenol derivatives: An approach to molecular docking and antimicrobial assession was written by Mangasuli, Sumitra N.;Managutti, Praveen B.;Hosamani, Kallappa M.;Joshi, Shrinivas D.. And the article was included in Chemical Data Collections in 2020.Quality Control of 4-Benzyloxyphenol The following contents are mentioned in the article:

A number of new substituted (2H-chromen-2-one)-phenol derivatives I [R = Me, Cl, Br, etc.] were synthesized by Williamson ether reaction follows an S_N² bimol. nucleophilic substitution mechanism. The titled compounds I was characterized by IR, ¹H NMR, ¹³C NMR and Mass spectral studies. As predicted, the derivatization of benzyloxy phenol with coumarin via ether linkage enhanced the activity of the titled compounds I against four bacterial and four fungal strains. Compound I [R = 1-naphthyloxy] showed significant strong anti-microbial broad spectrum activity against all tested bacterial and fungal strains. Anti-bacterial assay against standard coupled with in-silico mol. docking studies indicated that I [R = 1-naphthyloxy] showed promising activity with higher C-score values. This study involved multiple reactions and reactants, such as 4-Benzyloxyphenol (cas: 103-16-2Quality Control of 4-Benzyloxyphenol).

4-Benzyloxyphenol (cas: 103-16-2) belongs to ethers. Esters are widespread in nature and are widely used in industry. In nature, fats are in general triesters derived from glycerol and fatty acids. Esters are responsible for the aroma of many fruits. Liquid esters of low volatility serve as softening agents for resins and plastics. Esters also include many industrially important polymers. Polymethyl methacrylate is a glass substitute sold under the names Lucite and Plexiglas; polyethylene terephthalate is used as a film (Mylar) and as textile fibres sold as Terylene, Fortrel, and Dacron.Quality Control of 4-Benzyloxyphenol

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

Constructing chiral bicyclo[3.2.1]octanes via palladium-catalyzed asymmetric tandem Heck/carbonylation desymmetrization of cyclopentenes was written by Yuan, Zhenbo;Zeng, Yuye;Feng, Ziwen;Guan, Zhe;Lin, Aijun;Yao, Hequan. And the article was included in Nature Communications in 2020.Application of 103-16-2 The following contents are mentioned in the article:

A palladium-catalyzed asym. tandem Heck/carbonylation desymmetrization of cyclopentenes I (R = COMe, CO₂Et; R¹ = H, F, Cl, Me, OMe; X = I, Br) has been described. Alcs., (such as., n-propanol, isopropanol, cyclohexanol, etc.) phenols (such as., 4-methylphenol, biphenyl-4-ol, naphthol, etc.) and amines (such as., pyrrolidine, morpholine, benzylamine, etc.) are employed as versatile coupling reagents for the construction of multifunctional chiral bicyclo[3.2.1]octanes II (R² = OMe, OEt, OPh, pyrrolidino, morpholino, thiomorpholino, etc.) with one all-carbon quaternary and two tertiary carbon stereogenic centers in high diastereo- and enantioselectivities. This study represents an important progress in both the asym. tandem Heck/carbonylation reactions and enantioselective difunctionalization of internal alkenes. This study involved multiple reactions and reactants, such as 4-Benzyloxyphenol (cas: 103-16-2Application of 103-16-2).

4-Benzyloxyphenol (cas: 103-16-2) belongs to ethers. Carboxylic acid esters of low molecular weight are colourless, volatile liquids with pleasant odours, slightly soluble in water. Esters contain a carbonyl center, which gives rise to 120° C–C–O and O–C–O angles. Unlike amides, esters are structurally flexible functional groups because rotation about the C–O–C bonds has a low barrier. Their flexibility and low polarity is manifested in their physical properties; they tend to be less rigid (lower melting point) and more volatile (lower boiling point) than the corresponding amides. Application of 103-16-2

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

Constructing chiral bicyclo[3.2.1]octanes via palladium-catalyzed asymmetric tandem Heck/carbonylation desymmetrization of cyclopentenes was written by Yuan, Zhenbo;Zeng, Yuye;Feng, Ziwen;Guan, Zhe;Lin, Aijun;Yao, Hequan. And the article was included in Nature Communications in 2020.Related Products of 103-16-2 The following contents are mentioned in the article:

A palladium-catalyzed asym. tandem Heck/carbonylation desymmetrization of cyclopentenes I (R = COMe, CO₂Et; R¹ = H, F, Cl, Me, OMe; X = I, Br) has been described. Alcs., (such as., n-propanol, isopropanol, cyclohexanol, etc.) phenols (such as., 4-methylphenol, biphenyl-4-ol, naphthol, etc.) and amines (such as., pyrrolidine, morpholine, benzylamine, etc.) are employed as versatile coupling reagents for the construction of multifunctional chiral bicyclo[3.2.1]octanes II (R² = OMe, OEt, OPh, pyrrolidino, morpholino, thiomorpholino, etc.) with one all-carbon quaternary and two tertiary carbon stereogenic centers in high diastereo- and enantioselectivities. This study represents an important progress in both the asym. tandem Heck/carbonylation reactions and enantioselective difunctionalization of internal alkenes. This study involved multiple reactions and reactants, such as 4-Benzyloxyphenol (cas: 103-16-2Related Products of 103-16-2).

4-Benzyloxyphenol (cas: 103-16-2) belongs to ethers. Esters typically have a pleasant smell; those of low molecular weight are commonly used as fragrances and are found in essential oils and pheromones. Esters contain a carbonyl center, which gives rise to 120° C–C–O and O–C–O angles. Unlike amides, esters are structurally flexible functional groups because rotation about the C–O–C bonds has a low barrier. Their flexibility and low polarity is manifested in their physical properties; they tend to be less rigid (lower melting point) and more volatile (lower boiling point) than the corresponding amides. Related Products of 103-16-2

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

Photoconductive bent-core liquid crystalline radicals with a paramagnetic polar switchable phase was written by Shivakumar, Kilingaru I.;Pociecha, Damian;Szczytko, Jacek;Kapuscinski, Szymon;Monobe, Hirosato;Kaszynski, Piotr. And the article was included in Journal of Materials Chemistry in 2020.Related Products of 103-16-2 The following contents are mentioned in the article:

A series of self-organizing bent-core derivatives 1[12,n] (I; n = 10, 12, 14, 16) containing a highly π-delocalized stable radical as the central angular structural element, is described. The planarity of the open-shell core permits efficient π-π stacking, which results in the formation of B2 and soft crystalline phases above 100°C. Optical, XRD and dielec. analyses of 1[12,12] indicate that the ground state of the observed B2 phase is polar antiferroelec. of type SmC_AP_A exhibiting tristable electro-optical switching. SQUID and EPR measurements revealed strong antiferromagnetic spin-spin exchange interactions below the isotropic phase, which have been estimated at θ = -46 cm^-1 with the Curie-Weiss law. Transient photoconductivity was observed in the B2 phase with a hole carrier mobility μ_h of 1.4 × 10^-4 cm² V^-1 s^-1. This study involved multiple reactions and reactants, such as 4-Benzyloxyphenol (cas: 103-16-2Related Products of 103-16-2).

4-Benzyloxyphenol (cas: 103-16-2) belongs to ethers. Esters perform as high-grade solvents for a broad array of plastics, plasticizers, resins, and lacquers, and are one of the largest classes of synthetic lubricants on the commercial market. Liquid esters of low volatility serve as softening agents for resins and plastics. Esters also include many industrially important polymers. Polymethyl methacrylate is a glass substitute sold under the names Lucite and Plexiglas; polyethylene terephthalate is used as a film (Mylar) and as textile fibres sold as Terylene, Fortrel, and Dacron.Related Products of 103-16-2

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

Photoconductive bent-core liquid crystalline radicals with a paramagnetic polar switchable phase was written by Shivakumar, Kilingaru I.;Pociecha, Damian;Szczytko, Jacek;Kapuscinski, Szymon;Monobe, Hirosato;Kaszynski, Piotr. And the article was included in Journal of Materials Chemistry in 2020.Product Details of 103-16-2 The following contents are mentioned in the article:

A series of self-organizing bent-core derivatives 1[12,n] (I; n = 10, 12, 14, 16) containing a highly π-delocalized stable radical as the central angular structural element, is described. The planarity of the open-shell core permits efficient π-π stacking, which results in the formation of B2 and soft crystalline phases above 100°C. Optical, XRD and dielec. analyses of 1[12,12] indicate that the ground state of the observed B2 phase is polar antiferroelec. of type SmC_AP_A exhibiting tristable electro-optical switching. SQUID and EPR measurements revealed strong antiferromagnetic spin-spin exchange interactions below the isotropic phase, which have been estimated at θ = -46 cm^-1 with the Curie-Weiss law. Transient photoconductivity was observed in the B2 phase with a hole carrier mobility μ_h of 1.4 × 10^-4 cm² V^-1 s^-1. This study involved multiple reactions and reactants, such as 4-Benzyloxyphenol (cas: 103-16-2Product Details of 103-16-2).

4-Benzyloxyphenol (cas: 103-16-2) belongs to ethers. Esters typically have a pleasant smell; those of low molecular weight are commonly used as fragrances and are found in essential oils and pheromones. Esters contain a carbonyl center, which gives rise to 120° C–C–O and O–C–O angles. Unlike amides, esters are structurally flexible functional groups because rotation about the C–O–C bonds has a low barrier. Their flexibility and low polarity is manifested in their physical properties; they tend to be less rigid (lower melting point) and more volatile (lower boiling point) than the corresponding amides. Product Details of 103-16-2

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

Synthesis and activity of BNF15 against drug-resistant Mycobacterium tuberculosis was written by Mahmud, Hafij Al;Seo, Hoonhee;Kim, Sukyung;Islam, Imtiazul Md;Sultana, Omme Fatema;Nam, Kung-Woo;Lee, Byung-Eui;Sadu, Venkata S.;Lee, Kee-In;Song, Ho-Yeon. And the article was included in Future Medicinal Chemistry in 2021.Synthetic Route of C13H12O2 The following contents are mentioned in the article:

Tuberculosis is the leading cause of mortality among infectious diseases worldwide. Finding a new competent anti tubercular therapy is essential. We screened thousands of compounds and evaluated their efficacy against Mycobacterium tuberculosis. Initially, 2- nitronaphtho[2,3-b]benzofuran-6,11-dione was active against M. tuberculosis. Next, among 15 newly synthesized derivatives, BNF15 showed promising effect against all drug-sensitive and drug-resistant M. tuberculosis (MIC: 0.02-0.78 μg/mL). BNF15 effectively killed intracellular M. tuberculosis and nontuberculous mycobacteria. BNF15 exhibited a prolonged post antibiotic effect superior to isoniazid, streptomycin, and ethambutol and synergistic interaction with rifampicin. In acute oral toxicity test, BNF15 did not show toxic effect at a concentration up to 2000 mg/kg. These results highlight the perspective of BNF15 to treat drug-resistant M. tuberculosis. This study involved multiple reactions and reactants, such as 4-Benzyloxyphenol (cas: 103-16-2Synthetic Route of C13H12O2).

4-Benzyloxyphenol (cas: 103-16-2) belongs to ethers. Esters perform as high-grade solvents for a broad array of plastics, plasticizers, resins, and lacquers, and are one of the largest classes of synthetic lubricants on the commercial market. Because of their lack of hydrogen-bond-donating ability, esters do not self-associate. Consequently, esters are more volatile than carboxylic acids of similar molecular weight.Synthetic Route of C13H12O2

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

Synthesis and activity of BNF15 against drug-resistant Mycobacterium tuberculosis was written by Mahmud, Hafij Al;Seo, Hoonhee;Kim, Sukyung;Islam, Imtiazul Md;Sultana, Omme Fatema;Nam, Kung-Woo;Lee, Byung-Eui;Sadu, Venkata S.;Lee, Kee-In;Song, Ho-Yeon. And the article was included in Future Medicinal Chemistry in 2021.Name: 4-Benzyloxyphenol The following contents are mentioned in the article:

Tuberculosis is the leading cause of mortality among infectious diseases worldwide. Finding a new competent anti tubercular therapy is essential. We screened thousands of compounds and evaluated their efficacy against Mycobacterium tuberculosis. Initially, 2- nitronaphtho[2,3-b]benzofuran-6,11-dione was active against M. tuberculosis. Next, among 15 newly synthesized derivatives, BNF15 showed promising effect against all drug-sensitive and drug-resistant M. tuberculosis (MIC: 0.02-0.78 μg/mL). BNF15 effectively killed intracellular M. tuberculosis and nontuberculous mycobacteria. BNF15 exhibited a prolonged post antibiotic effect superior to isoniazid, streptomycin, and ethambutol and synergistic interaction with rifampicin. In acute oral toxicity test, BNF15 did not show toxic effect at a concentration up to 2000 mg/kg. These results highlight the perspective of BNF15 to treat drug-resistant M. tuberculosis. This study involved multiple reactions and reactants, such as 4-Benzyloxyphenol (cas: 103-16-2Name: 4-Benzyloxyphenol).

4-Benzyloxyphenol (cas: 103-16-2) belongs to ethers. Esters perform as high-grade solvents for a broad array of plastics, plasticizers, resins, and lacquers, and are one of the largest classes of synthetic lubricants on the commercial market. Esterification is the general name for a chemical reaction in which two reactants (typically an alcohol and an acid) form an ester as the reaction product. Esters are common in organic chemistry and biological materials.Name: 4-Benzyloxyphenol

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

Boric Acid as a Novel Homogeneous Catalyst Coupled with Ru/C for Hydrodeoxygenation of Phenolic Compounds and Raw Lignin Oil was written by Luo, Bowen;Li, Rongxuan;Shu, Riyang;Wang, Chao;Zhang, Jingtao;Chen, Ying. And the article was included in Industrial & Engineering Chemistry Research in 2020.HPLC of Formula: 103-16-2 The following contents are mentioned in the article:

Simple and efficient catalytic routes have been explored to upgrade the raw lignin oil. Though homogeneous catalysis is easy to operate and possesses a high reaction rate, it also suffers from the difficulty of product separation In this work, we used H₃BO₃ as a novel homogeneous catalyst coupled with Ru/C to overcome the separation problem and carry out the hydrodeoxygenation (HDO) of phenolic compounds and raw lignin oil. H₃BO₃ showed an outstanding performance over the liquid organic and mineral acids, with a good catalyst recyclability. Phenolic model compounds including monomers and dimers can be efficiently converted into cycloalkanes with yields close to 100%. Moreover, the raw lignin oil also had a good HDO result by using this bifunctional catalyst (H₃BO₃ and Ru/C). The content of hydrocarbons increased from 7.9% to 93.1% at 260°C, which promoted the upgraded lignin oil capable to be used as fuel directly. This study involved multiple reactions and reactants, such as 4-Benzyloxyphenol (cas: 103-16-2HPLC of Formula: 103-16-2).

4-Benzyloxyphenol (cas: 103-16-2) belongs to ethers. Esters typically have a pleasant smell; those of low molecular weight are commonly used as fragrances and are found in essential oils and pheromones. Esters are more polar than ethers but less polar than alcohols. They participate in hydrogen bonds as hydrogen-bond acceptors, but cannot act as hydrogen-bond donors, unlike their parent alcohols. This ability to participate in hydrogen bonding confers some water-solubility.HPLC of Formula: 103-16-2

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