Archives for Chemistry Experiments of Sodium 4-(propoxycarbonyl)phenolate

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35285-69-9, Name is Sodium 4-(propoxycarbonyl)phenolate, molecular formula is C10H11NaO3, belongs to isothiazole compound, is a common compound. In a patnet, author is Hao, Junliang, once mentioned the new application about 35285-69-9, Computed Properties of C10H11NaO3.

Discovery of (1R,2R)-N-(4-(6-isopropylpyridin-2-yl)-3-(2-methyl-2H-indazol-5-yl)isothiazol-5-yl)-2-methylcyclopropanecarboxamide, a potent and orally efficacious mGlu5 receptor negative allosteric modulator

A novel series of selective negative allosteric modulators (NAMs) for metabotropic glutamate receptor 5 (mGlu5) was discovered from an isothiazole scaffold. One compound of this series, (1R,2R)-N-(4-(6-isopropylpyridin-2-yl)-3-(2-methyl-2H-indazol-5-yl)isothiazol-5-yl)-2-methylcyclopropanecarboxamide (24), demonstrated satisfactory pharmacokinetic properties and, following oral dosing in rats, produced dose-dependent and long-lasting mGlu5 receptor occupancy. Consistent with the hypothesis that blockade of mGlu5 receptors will produce analgesic effects in mammals, compound 24 produced a dose-dependent reduction in paw licking responses in the formalin model of persistent pain. (c) 2013 Elsevier Ltd. All rights reserved.

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Reference:
Isothiazole – Wikipedia,
,Isothiazole – ScienceDirect.com

 

Archives for Chemistry Experiments of 35285-69-9

Reference of 35285-69-9, Because enzymes can increase reaction rates by enormous factors and tend to be very specific, typically producing only a single product in quantitative yield, they are the focus of active research.you can also check out more blogs about 35285-69-9.

Reference of 35285-69-9, The transformation of simple hydrocarbons into more complex and valuable products via catalytic C¨CH bond functionalisation has revolutionised modern synthetic chemistry. 35285-69-9, Name is Sodium 4-(propoxycarbonyl)phenolate, SMILES is [O-]C1=CC=C(C(OCCC)=O)C=C1.[Na+], belongs to isothiazole compound. In a article, author is Bumagin, N. A., introduce new discover of the category.

Functionalized isoxazole and isothiazole ligands: design, synthesis, palladium complexes, homogeneous and heterogeneous catalysis in aqueous media

Homogenous and heterogeneous palladium catalysts with functionalized izoxazole and isothiazole ligands were developed for the cross-coupling reactions. The catalysts possessed high activity and were suitable for the repeated use. Compared with commonly used organic solutions, application of water and its mixtures with methanol as a reaction medium significantly intensifies catalysis with no side being formed. The obtained results are promising for the development of effective and ecologically friendly technologies of synthesis of important compounds such as polyfunctional biaryls, arylated olefins, acetylenes and their heterocyclic analogs.

Reference of 35285-69-9, Because enzymes can increase reaction rates by enormous factors and tend to be very specific, typically producing only a single product in quantitative yield, they are the focus of active research.you can also check out more blogs about 35285-69-9.

Reference:
Isothiazole – Wikipedia,
,Isothiazole – ScienceDirect.com

 

The Absolute Best Science Experiment for Sodium 4-(propoxycarbonyl)phenolate

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Chemo-enzymatic cascade processes are invaluable due to their ability to rapidly construct high-value products from available feedstock chemicals in a one-pot relay manner. In an article, author is Incerti, Matteo, once mentioned the application of 35285-69-9, Name is Sodium 4-(propoxycarbonyl)phenolate, molecular formula is C10H11NaO3, molecular weight is 202.18, MDL number is MFCD00016477, category is isothiazole. Now introduce a scientific discovery about this category, Formula: C10H11NaO3.

Complete H-1 and C-13 NMR spectral assignment of benzo[d]isothiazole derivatives and of an isoindole isoster

The complete H-1 and C-13 NMR assignments of the novel compound methyl 2-amino-3-(benzo[d]isothiazol-3-yl)propanoate (1), of 3-amino-5-methylbenzo[d]isothiazole (2) and N-(t-butyloxycarbonyl)-2-aminobenzo[d]isothiazol-3(2H)-one (3) and of the desulfurated isostere of 3, N-(t-butyloxycarbonyl)-2-aminoisoindolin-1 -one (4), using 1D and 2D NMR techniques, including COSY, INADEQUATE, HSQC, and HMBC experiments are reported. Copyright (C) 2008 John Wiley & Sons, Ltd.

Do you like my blog? If you like, you can also browse other articles about this kind. Thanks for taking the time to read the blog about 35285-69-9, Formula: C10H11NaO3.

Reference:
Isothiazole – Wikipedia,
,Isothiazole – ScienceDirect.com

 

Brief introduction of 35285-69-9

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A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, Product Details of 35285-69-9, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 35285-69-9, Name is Sodium 4-(propoxycarbonyl)phenolate, molecular formula is C10H11NaO3. In an article, author is Lippa, B,once mentioned of 35285-69-9.

Discovery of novel isothiazole inhibitors of the TrkA kinase: Structure-activity relationship, computer modeling, optimization, and identification of highly potent antagonists

The design, synthesis, and biological evaluation of potent inhibitors of the TrkA kinase is presented. A homology model is created to aid in the enhancement of potency and selectivity of isothiazole inhibitors found during a high-throughput screen. Three different syntheses are utilized to make diverse analogs within this series. Aminoheterocycles are found to be good urea surrogates, whereas bicyclic substituents on the C3 thio group were found to be extremely potent TrkA inhibitors in kinase and cell assays. (c) 2006 Elsevier Ltd. All rights reserved.

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Reference:
Isothiazole – Wikipedia,
,Isothiazole – ScienceDirect.com