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2-(2-aMinothiazol-4-yl)acetyl chloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

785723-55-9

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785723-55-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 785723-55-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,8,5,7,2 and 3 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 785723-55:
(8*7)+(7*8)+(6*5)+(5*7)+(4*2)+(3*3)+(2*5)+(1*5)=209
209 % 10 = 9
So 785723-55-9 is a valid CAS Registry Number.

785723-55-9Downstream Products

785723-55-9Relevant academic research and scientific papers

Synthesis, characterization and molecular docking studies of acetamide derivatives of 2-aminothiazole and 2-dihydropyridinone derivative of benzimidazole

Anbazhagan, V.,Britto, S.,Kanagasabapathy, G.

, (2022/01/13)

An efficient and easy synthesis of highly functionalized thiazole and pyridinone-substituted benzimidazole derivatives has been developed. The imino carbon of the benzimidazole derivative is coupled with the nitrogen atom of 1,4-dihydropyridinone and the aminothiazole-substituted acetic acid is condensed with two differently functionalized aniline, in two different reactions to form the amide linkages. These two amides and pyridinone-coupled benzimidazole are characterized by IR, 1H & 13C NMR and mass spectral studies. They are further evaluated for their antibacterial activity against the gram-positive bacterium Staphylococcus epidermidis and the fungus Saccharomyces cerevisiae by molecular docking method. All the three synthesized compounds had relatively lesser binding energy than what the standard drugs chloramphenicol and fluconazole have and may be considered as better inhibitors.

A PROCESS FOR THE PREPARATION OF MIRABEGRON AND ITS INTERMEDIATES

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Page/Page column 27-28, (2016/02/29)

The present invention relates to a novel process for preparation of Mirabegron of Formula (I) using intermediates of Formula (II), (IIIa), (Illb) and (IV).

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