Tag: 100-200

Safety of 2-MethoxybenzaldehydeIn 2019 ,《Synthesis of new low-viscous sulfonic acid-functionalized ionic liquid and its application as a Bronsted liquid acid catalyst for the one-pot mechanosynthesis of 4H-pyrans through the ball milling process》 appeared in Journal of Molecular Liquids. The author of the article were Khaligh, Nader Ghaffari; Mihankhah, Taraneh; Johan, Mohd. Rafie. The article conveys some information:

In the present study, a new low-viscous sulfonic acid-functionalized ionic liquid (SAIL) viz. 4,4′-trimethylene-N,N’-sulfonic acid-dipiperidinium chloride was synthesized and characterized by FTIR, 1D and 2D NMR, and Mass spectra. Then, some properties of new SAIL were determined including pH, viscosity, d., and solubility in some common solvents. The catalytic activity of new SAIL was demonstrated for the one-pot mechanosynthesis of pyrano[4,3-b]pyrans, dihydropyrano[3,2-c]chromene and tetrahydrobenzo[b]pyrans using planetary ball mill under solvent-free conditions. This current mechanosynthesis methodol. for the synthesis of 4H-pyran-annulated heterocyclic scaffolds displays a combination of the synthetic virtues of conventional multi-component reaction with ecol. benefits and convenience of a simple mechanocatalytic procedure. New SAIL was easily recycled and reused several times with no significant loss of activity. After reading the article, we found that the author used 2-Methoxybenzaldehyde(cas: 135-02-4Safety of 2-Methoxybenzaldehyde)

2-Methoxybenzaldehyde(cas: 135-02-4) is found in cassia oil, cinnamon bark, and cinnamon bark oil. It is a clear colorless liquid with a strong aroma. It has been used to examine the acaricidal activity of Periploca sepium oil and its active component against Tyrophagus putrescentiae.Safety of 2-Methoxybenzaldehyde

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Recommanded Product: N,N-Dimethylformamide Dimethyl AcetalIn 2020 ,《Discovery of BMS-986260, a Potent, Selective, and Orally Bioavailable TGFβR1 Inhibitor as an Immuno-oncology Agent》 appeared in ACS Medicinal Chemistry Letters. The author of the article were Velaparthi, Upender; Darne, Chetan Padmakar; Warrier, Jayakumar; Liu, Peiying; Rahaman, Hasibur; Augustine-Rauch, Karen; Parrish, Karen; Yang, Zheng; Swanson, Jesse; Brown, Jennifer; Dhar, Gopal; Anandam, Aravind; Holenarsipur, Vinay K.; Palanisamy, Kamalavenkatesh; Wautlet, Barri S.; Fereshteh, Mark P.; Lippy, Jonathan; Tebben, Andrew J.; Sheriff, Steven; Ruzanov, Max; Yan, Chunhong; Gupta, Anuradha; Gupta, Arun Kumar; Vetrichelvan, Muthalagu; Mathur, Arvind; Gelman, Marina; Singh, Rajinder; Kinsella, Todd; Murtaza, Anwar; Fargnoli, Joseph; Vite, Gregory; Borzilleri, Robert M.. The article conveys some information:

Novel imidazole-based TGFβR1 inhibitors were identified and optimized for potency, selectivity, and pharmacokinetic and physicochem. characteristics. Herein, we report the discovery, optimization, and evaluation of a potent, selective, and orally bioavailable TGFβR1 inhibitor, 10 (BMS-986260). This compound demonstrated functional activity in multiple TGFβ-dependent cellular assays, excellent kinome selectivity, favorable pharmacokinetic properties, and curative in vivo efficacy in combination with anti-PD-1 antibody in murine colorectal cancer (CRC) models. Since daily dosing of TGFβR1 inhibitors is known to cause class-based cardiovascular (CV) toxicities in preclin. species, a dosing holiday schedule in the anti-PD-1 combination efficacy studies was explored. An intermittent dosing regimen of 3 days on and 4 days off allowed mitigation of CV toxicities in one month dog and rat toxicol. studies and also provided similar efficacy as once daily dosing. The experimental process involved the reaction of N,N-Dimethylformamide Dimethyl Acetal(cas: 4637-24-5Recommanded Product: N,N-Dimethylformamide Dimethyl Acetal)

N,N-Dimethylformamide Dimethyl Acetal(cas: 4637-24-5) belongs to anime. Reaction with nitrous acid (HNO2), which functions as an acylating agent that is a source of the nitrosyl group (―NO), converts aliphatic primary amines to nitrogen and mixtures of alkenes and alcohols corresponding to the alkyl group in a complex process. This reaction has been used for analytical determination of primary amino groups in a procedure known as the Van Slyke method.Recommanded Product: N,N-Dimethylformamide Dimethyl Acetal

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Ether – Wikipedia,
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In 2022,Zhu, Longfei; Ye, Sen; Zhu, Jiazheng; Duan, Chengjie; Li, Kun; He, Guangke; Liu, Xiang published an article in ACS Sustainable Chemistry & Engineering. The title of the article was 《Tartaric Acid-Assisted Synthesis of Well-Dispersed Ni Nanoparticles Supported on Hydroxyapatite for Efficient Phenol Hydrogenation》.Computed Properties of C7H8O2 The author mentioned the following in the article:

Developing highly active nonnoble-metal-based heterogeneous catalysts for selective hydrogenation is a long-sought goal due to the scarcity and high price of noble metals. Herein, well-dispersed and small-sized Ni nanoparticles (NPs) supported on hydroxyapatite (Ni-TA/HAP) were prepared using a simple tartaric acid (TA)-assisted impregnation method, which is based on the coupling interaction of strong electrostatic adsorption between the HAP and TA and reactive metal-ligand chelation between Ni and TA. Under mild conditions (e.g., 1 mol % Ni, 3 bar H2 at 80°C), the as-synthesized Ni-TA/HAP exhibited excellent activity and selectivity (>99%) for the efficient hydrogenation of phenolic compounds to the corresponding cyclohexanols, as well as the controlled partial hydrogenation of N-heteroarenes. Characterization results revealed that TA addition could promote a better dispersion of Ni species and inhibit the aggregation of Ni NPs during the fabrication of the Ni-TA/HAP catalyst. An optimal TA dosage (nTA/nNi = 0.5) as well as a low Ni loading (1.0 weight %) coconstructed the favorable microstructure of the well-dispersed Ni nanoparticles as the catalytic center. The hydrogenation was boosted by small-sized Ni nanoparticles with a high ability for H2 activation and HAP with both base and acid sites for appreciating phenol absorption. The experimental part of the paper was very detailed, including the reaction process of m-Methoxyphenol(cas: 150-19-6Computed Properties of C7H8O2)

m-Methoxyphenol(cas: 150-19-6) may be used as an analytical standard for the determination of the analyte in wine, coffee beans, wood samples, and mainstream smoke by gas chromatography (GC) based techniques.Computed Properties of C7H8O2

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

In 2022,Cartagenova, Daniele; Bachmann, Stephan; Puntener, Kurt; Scalone, Michelangelo; Newton, Mark A.; Peixoto Esteves, Fabio A.; Rohrbach, Thomas; Zimmermann, Patrik P.; van Bokhoven, Jeroen A.; Ranocchiari, Marco published an article in Catalysis Science & Technology. The title of the article was 《Highly selective Suzuki reaction catalyzed by a molecular Pd-P-MOF catalyst under mild conditions: role of ligands and palladium speciation》.Synthetic Route of C7H7BrO The author mentioned the following in the article:

A molecularly-defined heterogeneous palladium catalyst based on a phosphine-metal-organic framework (P-MOF) ligand system was reported. This catalyst performed Suzuki reactions of aryl bromides and Ph boronic acid to afford biaryls R-R1 [R = Ph; R1 = 3-MeC6H4, 3-OMeC6H4, 3-pyridyl, etc.] in exceptionally mild conditions while displayed a unique selectivity, higher than that achieved using Pd(PPh3)4, a standard homogeneous catalyst. The new palladium P-MOF catalyst was active for a wide range of substrates. Determination of the palladium speciation showed that molecularly-defined palladium-phosphine sites catalyzed the Suzuki cross-coupling with very high selectivity, and that, when formed, palladium nanoparticles promoted hydrodehalogenation. The fraction of molecularly defined palladium was maximized by having excess of phosphine ligand in the system. After reading the article, we found that the author used 1-Bromo-3-methoxybenzene(cas: 2398-37-0Synthetic Route of C7H7BrO)

1-Bromo-3-methoxybenzene(cas: 2398-37-0) can be used in chemical reaction as intermediates to obtain target materials such as dyes, pharmaceuticals, perfumes, photoinitiators and agrochemicals.Synthetic Route of C7H7BrO

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

In 2022,Afari, Mark N. K.; Virta, Pasi; Lonnberg, Tuomas published an article in Organic & Biomolecular Chemistry. The title of the article was 《N-Methoxy-1,3-oxazinane nucleic acids (MOANAs) – a configurationally flexible backbone modification allows post-synthetic incorporation of base moieties》.Electric Literature of C9H10O2 The author mentioned the following in the article:

(2R,3S)-4-(Methoxyamino)butane-1,2,3-triol was converted into a protected phosphoramidite building block and incorporated into the middle of a short DNA oligonucleotide. O1 and O3 of the (2R,3S)-4-(methoxyamino)butane-1,2,3-triol were engaged in phosphodiester linkages, leaving O2 and the methoxyamino function available to form an N-methoxy-1,3-oxazinane ring through reaction with an aldehyde. In modified oligonucleotides thus obtained, the oxazinane ring formally replaces the furanose ring and the aldehyde, the base moiety of natural nucleosides. The feasibility of synthesizing base-modified oligonucleotides by this approach was demonstrated with several aromatic and aliphatic aldehydes featuring various functional groups. The experimental part of the paper was very detailed, including the reaction process of 2-(Benzyloxy)acetaldehyde(cas: 60656-87-3Electric Literature of C9H10O2)

2-(Benzyloxy)acetaldehyde(cas: 60656-87-3) is a non-natural aldehyde. It undergoes enantioselective Mukaiyama aldol reaction with silylketene acetal nucleophiles in the presence of C2-symmetric bis(oxazolinyl)pyridine Cu(II) complex (catalyst).Electric Literature of C9H10O2

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

In 2022,Gutierrez, Mario; Garcia, Eduardo; Monterde, Cristina; Sanchez, Felix; Douhal, Abderrazzak published an article in Physical Chemistry Chemical Physics. The title of the article was 《Modulating the spectroscopy and dynamics of a proton-transfer dye by functionalizing with phenyl groups》.COA of Formula: C8H8O2 The author mentioned the following in the article:

Mols. undergoing excited-state proton transfer (ESPT) reactions are among the most interesting systems from spectroscopic and photophys. viewpoints. These mols. can be further functionalized with electron donating or accepting groups, inducing intramol. charge transfer (ICT) events, which might be coupled to the ESIPT ones, conferring them with different spectroscopic and photophys. properties, which can be essential to implement the related materials in many key scientific and technol. fields. Here, authors report new benzimidazole derivatives that are functionalized with a Ph group, 2-(5,10-diphenyl-1H-phenanthro[9,10-d]imidazol-2-yl)phenol (DP-HPPI), and its methylated equivalent, 2-(2-methoxyphenyl)-5,10-diphenyl-1H-phenanthro[9,10-d]imidazole (DP-MPPI). The results prove that these mols. in solutions undergo an ultrafast ICT (400-700 fs) reaction. Addnl., DP-HPPI also undergoes a reversible ESIPT process in dichloromethane. However, this is precluded in acetonitrile due to the involvement of intermol. H-bonds in this solvent. These results provide key insights into the development of proton-transfer materials with bespoke spectral and photodynamical properties. In the experiment, the researchers used many compounds, for example, 2-Methoxybenzaldehyde(cas: 135-02-4COA of Formula: C8H8O2)

2-Methoxybenzaldehyde(cas: 135-02-4) is used as a flavor agent in foods including nonalcoholic/alcoholic beverages, baked goods, chewing gum, confections, frozen dairy, fruit ices, hard/soft candy, instant coffee, tea, Jams, jellies, and milk products. It also has been used to obtain good enantioselectivities using Cu(OAc)(2)-bis(oxazolines) via hydrogen bonding in asymmetric Henry reaction.COA of Formula: C8H8O2

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

In 2022,Lakshmidevi, Jangam; Naidu, Bandameeda Ramesh; Reddy, S. Siva Sankara; Venkateswarlu, Katta published an article in Waste and Biomass Valorization. The title of the article was 《Oxidative Iododeborylation Reaction of (Hetero)arylboronic Acids in Water Extract of Pomegranate Ash: A Novel and Sustainable Synthesis of Iodo(hetero)arenes》.Category: ethers-buliding-blocks The author mentioned the following in the article:

A mild and effective process for the (H)AIs synthesis RI (R = 4-nitrophenyl, 2-methoxyphenyl, pyridin-3-yl, etc.) via ipso-functionalization of (H)ABAs RB(OH)2using water extract of pomegranate peel ash (WEPA) and environmentally benign iodinating agent such as mol. iodine (I2) under external oxidant/(transition)metal/base/additive/organic solvent-free conditions have been disclosed. The (H)AIs are formed with high regioselctivity using this protocol that operational simplicity and displays exceptional functional group compatibility. Present (H)AIs synthesis avoid addnl. substances (including metals) as oxidizing reagents, additives/surfactants and catalysts, thus making this procedure as a highly sustainable asset using biorenewable waste based aqueous extract as catalytic media. In the part of experimental materials, we found many familiar compounds, such as 3-Methoxyphenylboronic acid(cas: 10365-98-7Category: ethers-buliding-blocks)

3-Methoxyphenylboronic acid(cas: 10365-98-7) belongs to boronic acids. Boronic acids are mild Lewis acids which are generally stable and easy to handle, making them important to organic synthesis.Category: ethers-buliding-blocks

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Ether – Wikipedia,
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Yu, Jianjin; Li, Chao-Jun; Zeng, Huiying published an article in 2021. The article was titled 《Dearomatization-Rearomatization Strategy for ortho-Selective Alkylation of Phenols with Primary Alcohols》, and you may find the article in Angewandte Chemie, International Edition.Category: ethers-buliding-blocks The information in the text is summarized as follows:

Phenols are common precursors and core structures of a variety of industrial chems. ranging from pharmaceuticals to polymers. However, the synthesis of site-specifically substituted phenols is challenging, and thus the development of new methods for this purpose would be highly desirable. Reported here is a protocol for palladium-catalyzed ortho-selective alkylation reactions of phenols with primary alcs. by a dearomatization-rearomatization strategy, with water as the sole byproduct. Various substituted phenols and primary alcs. were compatible with the standard reaction conditions. The detailed mechanism of this transformation was also investigated. After reading the article, we found that the author used m-Methoxyphenol(cas: 150-19-6Category: ethers-buliding-blocks)

m-Methoxyphenol(cas: 150-19-6) may be used as an analytical standard for the determination of the analyte in wine, coffee beans, wood samples, and mainstream smoke by gas chromatography (GC) based techniques.Category: ethers-buliding-blocks

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

Gu, Weijie; Martinez, Sergio; Singh, Abhimanyu K.; Nguyen, Hoai; Rozenski, Jef; Schols, Dominique; Herdewijn, Piet; Das, Kalyan; De Jonghe, Steven published an article in 2021. The article was titled 《Exploring the dNTP -binding site of HIV-1 reverse transcriptase for inhibitor design》, and you may find the article in European Journal of Medicinal Chemistry.Recommanded Product: 60656-87-3 The information in the text is summarized as follows:

HIV-1 reverse transcriptase (RT) plays a central role in the viral life cycle, and roughly half of the FDA-approved anti-HIV drugs are targeting RT. Nucleoside analogs (NRTIs) require cellular phosphorylation for binding to RT, and to bypass this rate-limiting path, we designed a new series of acyclic nucleoside phosphonate analogs as nucleoside triphosphate mimics, aiming at the chelation of the catalytic Mg2+ ions via a phosphonate and/or a carboxylic acid group. Novel synthetic procedures were developed to access these nucleoside phosphonate analogs. X-ray structures in complex with HIV-1 RT/dsDNA demonstrated that their binding modes are distinct from that of our previously reported compound series. The impact of chain length, chirality and linker atom have been discussed. The detailed structural understanding of these new compounds provides opportunities for designing new class of HIV-1 RT inhibitors. After reading the article, we found that the author used 2-(Benzyloxy)acetaldehyde(cas: 60656-87-3Recommanded Product: 60656-87-3)

2-(Benzyloxy)acetaldehyde(cas: 60656-87-3) is a non-natural aldehyde. It undergoes enantioselective Mukaiyama aldol reaction with silylketene acetal nucleophiles in the presence of C2-symmetric bis(oxazolinyl)pyridine Cu(II) complex (catalyst).Recommanded Product: 60656-87-3

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

Xavier, Tania; Pichon, Christophe; Presset, Marc; Le Gall, Erwan; Condon, Sylvie published an article in 2021. The article was titled 《Efficient Preparation of Methyl 2-Oxo-3-aryl (heteroaryl)-2H-pyran-5-carboxylate via Pd-Catalyzed Negishi Coupling》, and you may find the article in European Journal of Organic Chemistry.Application In Synthesis of 1-Bromo-3-methoxybenzene The information in the text is summarized as follows:

Me 3-bromocoumalate, readily obtained from Me 2-pyrone-5-carboxylate (Me coumalate), is easily substituted by cross-coupling reactions with arylzinc reagents ArZnBr (R = Ph, 3-acetylphenyl, thiophen-2-yl, etc.) under palladium catalysis, leading to Me 2-oxo-3-aryl (heteroaryl)-2H-pyran-5-carboxylates I. In the part of experimental materials, we found many familiar compounds, such as 1-Bromo-3-methoxybenzene(cas: 2398-37-0Application In Synthesis of 1-Bromo-3-methoxybenzene)

1-Bromo-3-methoxybenzene(cas: 2398-37-0) can be used in chemical reaction as intermediates to obtain target materials such as dyes, pharmaceuticals, perfumes, photoinitiators and agrochemicals.Application In Synthesis of 1-Bromo-3-methoxybenzene

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