Category: 767-68-0

A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 767-68-0, Name is 4-Bromobenzothiazole, molecular formula is C7H4BrNS. In a Patent£¬once mentioned of 767-68-0, name: 4-Bromobenzothiazole

The present application relates to novel cycloalkoxy-substituted 4-phenyl-3,5-dicyanopyridine derivatives, to processes for their preparation, to their use for the treatment and/or prevention of diseases and to their use for preparing medicaments for the treatment and/or prevention of diseases, preferably for the treatment and/or prevention of cardiovascular and metabolic disorders.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.name: 4-Bromobenzothiazole. In my other articles, you can also check out more blogs about 767-68-0

Reference£º
Thiazole | C3H5207NS – PubChem,
Thiazole | chemical compound | Britannica

Synthetic Route of 767-68-0, An article , which mentions 767-68-0, molecular formula is C7H4BrNS. The compound – 4-Bromobenzothiazole played an important role in people’s production and life.

This publication describes a highly selective oxidation of aldehydes to the corresponding acids or esters. The reaction proceeds under metal-free conditions by using N-heterocyclic carbenes as organocatalysts in combination with environmentally friendly oxygen as the terminal oxidation agent.

This publication describes a highly selective oxidation of aldehydes to the corresponding acids or esters. The reaction proceeds under metal-free conditions by using N-heterocyclic carbenes as organocatalysts in combination with environmentally friendly oxygen as the terminal oxidation agent.

I hope this article can help some friends in scientific research. I am very proud of our efforts over the past few months and hope to 767-68-0, help many people in the next few years., Synthetic Route of 767-68-0

Reference£º
Thiazole | C3H5196NS – PubChem,
Thiazole | chemical compound | Britannica

In an article, published in an article, once mentioned the application of 767-68-0, Name is 4-Bromobenzothiazole,molecular formula is C7H4BrNS, is a conventional compound. this article was the specific content is as follows.SDS of cas: 767-68-0

Mono-cationic Ru(II)-complexes [Ru(L)X(CH3CN)2]?X 1?4 (1, L = 2,6-bis(benzimidazol-2-yl) pyridine (L1), X = Cl; 2, L = L1, X = OTf; 3, L = 2-(N-benzyl-benzimidazole-2-yl)-6-(benzimidazole-2-yl)pyridine (L2), X = Cl; 4, L = 2,6-bis(N-benzyl-benzimidazole-2-yl)pyridine (L3), X = Cl) were prepared and fully characterized. The two acetonitrile ligands of each complex are coordinated to the metal center cis to each other. Complex 2 was also structurally characterized by X-ray crystallography. It was found that complexes 1?4 can catalyze the acceptorless dehydrogenation of primary alcohols to corresponding carboxylic acids and H2in the basic aqueous solution, and the reactivity follows the order 1 = 2 > 4 > 3. Furthermore, complexes 1 or 2 can efficiently catalyze the conversion of various primary alcohols to carboxylic acid in good yields (72%?98%) and high selectivity in an alcohol/CsOH system (1/1, mol/mol). Using an excess amount of alcohol to CsOH results in the formation of the carboxylic acid in higher yield (up to 100%, based on CsOH) and higher turnover numbers (TON ? 10000) accompanied by the H2evolution. Complexes 1 and 2 can act as a new class of phosphine- and N-heterocycle carbene free Ru(II) complexes for efficient conversion of primary alcohols to carboxylic acids and H2in a homogeneous system.

Mono-cationic Ru(II)-complexes [Ru(L)X(CH3CN)2]?X 1?4 (1, L = 2,6-bis(benzimidazol-2-yl) pyridine (L1), X = Cl; 2, L = L1, X = OTf; 3, L = 2-(N-benzyl-benzimidazole-2-yl)-6-(benzimidazole-2-yl)pyridine (L2), X = Cl; 4, L = 2,6-bis(N-benzyl-benzimidazole-2-yl)pyridine (L3), X = Cl) were prepared and fully characterized. The two acetonitrile ligands of each complex are coordinated to the metal center cis to each other. Complex 2 was also structurally characterized by X-ray crystallography. It was found that complexes 1?4 can catalyze the acceptorless dehydrogenation of primary alcohols to corresponding carboxylic acids and H2in the basic aqueous solution, and the reactivity follows the order 1 = 2 > 4 > 3. Furthermore, complexes 1 or 2 can efficiently catalyze the conversion of various primary alcohols to carboxylic acid in good yields (72%?98%) and high selectivity in an alcohol/CsOH system (1/1, mol/mol). Using an excess amount of alcohol to CsOH results in the formation of the carboxylic acid in higher yield (up to 100%, based on CsOH) and higher turnover numbers (TON ? 10000) accompanied by the H2evolution. Complexes 1 and 2 can act as a new class of phosphine- and N-heterocycle carbene free Ru(II) complexes for efficient conversion of primary alcohols to carboxylic acids and H2in a homogeneous system.

Do you like my blog? If you like, you can also browse other articles about this kind. SDS of cas: 767-68-0. Thanks for taking the time to read the blog about 767-68-0

Reference£º
Thiazole | C3H5214NS – PubChem,
Thiazole | chemical compound | Britannica

Children learn through play, and they learn more than adults might expect. Science experiments are a great way to spark their curiosity, get their minds active, and encourage them to do something that doesn¡¯t involve a screen. 767-68-0, C7H4BrNS. A document type is Patent, introducing its new discovery., category: thiazole

The present invention provides a novel SCD inhibitor. An SCD inhibitor containing a compound represented by the formula [I] [image] wherein ring A is an optionally substituted aromatic ring, ring B is an optionally substituted ring, ring C is an optionally substituted aromatic ring, R is a hydrogen atom, an optionally substituted hydrocarbon group or an optionally substituted heterocyclic group, and X is a spacer having 1 to 5 atoms in the main chain, or a salt thereof, or a prodrug thereof.

The present invention provides a novel SCD inhibitor. An SCD inhibitor containing a compound represented by the formula [I] [image] wherein ring A is an optionally substituted aromatic ring, ring B is an optionally substituted ring, ring C is an optionally substituted aromatic ring, R is a hydrogen atom, an optionally substituted hydrocarbon group or an optionally substituted heterocyclic group, and X is a spacer having 1 to 5 atoms in the main chain, or a salt thereof, or a prodrug thereof.

Interested yet? Keep reading other articles of 767-68-0!, category: thiazole

Reference£º
Thiazole | C3H5202NS – PubChem,
Thiazole | chemical compound | Britannica

In an article, published in an article, once mentioned the application of 767-68-0, Name is 4-Bromobenzothiazole,molecular formula is C7H4BrNS, is a conventional compound. this article was the specific content is as follows.Quality Control of: 4-Bromobenzothiazole

Compounds of formula (I) and their use in therapy, particularly for the treatment of a disorder responsive to inhibition of Aurora kinase A and/or B. Formula (I) wherein R 1 , R 2 , R 3 , R 4 and R 5 are independently selected from hydrogen, hydroxy, C 1 – C 3 alkyl, fluoro(C 1 -C 3 )alkyl, hydroxy(C 1 -C 3 )alkyl, C 1 -C 3 alkoxy, fluoro(C 1 – C 3 )alkoxy, hydroxyC 1 -C 3 alkoxy, -N(R 6 J-R 7 , – AIk-N(R 6 )-R 7 , -0-AIk-N(R 6 )-R 7 , – C(=O)OH, carboxy(C 1 -C 3 )alkyl, or -C(=O)-NH-R 8 ; R 6 , R 7 ,R 8 and -AIk- are as defined herein; R is hydrogen or C 1 C 3 alkyl; one of A and B is hydrogen and the other is a group -Z-Ar; -Z- is -C(=O)-NH-, -NH-C(=O)-, -C(=O)-N(-CH 3 )-, or -N(-CH 3 )-C(=O)-; and Ar is aryl or heteroaryl, optionally substituted with one or more halogen atoms, C 1 -C 3 alkyl radicals or trifluoromethyl radicals; or a pharmaceutically acceptable salt, hydrate or solvate thereof.

Compounds of formula (I) and their use in therapy, particularly for the treatment of a disorder responsive to inhibition of Aurora kinase A and/or B. Formula (I) wherein R 1 , R 2 , R 3 , R 4 and R 5 are independently selected from hydrogen, hydroxy, C 1 – C 3 alkyl, fluoro(C 1 -C 3 )alkyl, hydroxy(C 1 -C 3 )alkyl, C 1 -C 3 alkoxy, fluoro(C 1 – C 3 )alkoxy, hydroxyC 1 -C 3 alkoxy, -N(R 6 J-R 7 , – AIk-N(R 6 )-R 7 , -0-AIk-N(R 6 )-R 7 , – C(=O)OH, carboxy(C 1 -C 3 )alkyl, or -C(=O)-NH-R 8 ; R 6 , R 7 ,R 8 and -AIk- are as defined herein; R is hydrogen or C 1 C 3 alkyl; one of A and B is hydrogen and the other is a group -Z-Ar; -Z- is -C(=O)-NH-, -NH-C(=O)-, -C(=O)-N(-CH 3 )-, or -N(-CH 3 )-C(=O)-; and Ar is aryl or heteroaryl, optionally substituted with one or more halogen atoms, C 1 -C 3 alkyl radicals or trifluoromethyl radicals; or a pharmaceutically acceptable salt, hydrate or solvate thereof.

Do you like my blog? If you like, you can also browse other articles about this kind. Quality Control of: 4-Bromobenzothiazole. Thanks for taking the time to read the blog about 767-68-0

Reference£º
Thiazole | C3H5220NS – PubChem,
Thiazole | chemical compound | Britannica