19989-69-6

Basic information

• Product Name: 2-phenyl-1,3-benzothiazole-6-carboxylic acid
• Synonyms: 2-phenyl-1,3-benzothiazole-6-carboxylic acid
• CAS NO: 19989-69-6
• Molecular Weight: 255.297
• Mol File: 19989-69-6.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: 2-phenyl-1,3-benzothiazole-6-carboxylic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 2-phenyl-1,3-benzothiazole-6-carboxylic acid(19989-69-6)
• EPA Substance Registry System: 2-phenyl-1,3-benzothiazole-6-carboxylic acid(19989-69-6)

Safety Data

• Hazardous Substances Data: 19989-69-6(Hazardous Substances Data)

Upstream product

• 10205-58-0 6-methyl-2-phenyl-1,3-benzothiazole 
• 99073-88-8 ethyl 2-bromo-1,3-benzothiazole-6-carboxylate 
• 98-80-6 phenylboronic acid 
• 582-80-9 p-benzamidobenzoic acid 
• 14543-45-4 4-amino-3-mercaptobenzoic acid 
• 98-88-4 benzoyl chloride 
• 77333-68-7 2-phenylbenzo[d]thiazole-6-carbonitrile 
• 100-52-7 benzaldehyde 
• 19989-70-9 ethyl 2-phenylbenzo[d]thiazole-6-carboxylate 

Relevant articles and documents

Method used for rapid preparation of benzo-heterocycle compound with physical grinding under solvent-free room temperature conditions

The invention discloses a method used for rapid preparation of benzo-heterocycle compound with physical grinding under solvent-free room temperature conditions. According to the method, glacial aceticacid is taken as a catalyst; at solvent-free room temperature conditions, physical grinding is adopted, reaction of 2-substituted arylamines (2-mercapto arylamine, 2-aminophenol, and o-phenylenediamine) and aromatic aldehydes is carried out using physical grinding. The method is friendly to the environment, is simple in operation, is safe, is low in cost, and is high in efficiency. Compared withthe prior art, the advantages are that: the method is suitable for a large amount of functional groups, yield is high, less by-product is generated, operation is simple, the method is safe, cost is low, and the method is friendly to the environment.

OXOPIPERAZINE-AZETIDINE AMIDES AND OXODIAZEPINE-AZETIDINE AMIDES AS MONOACYLGLYCEROL LIPASE INHIBITORS

Disclosed are compounds, compositions and methods for treating various diseases, syndromes, conditions and disorders, including pain. Such compounds, and enantiomers, diastereomers, and pharmaceutically acceptable salts thereof, are represented by Formula (Ia) and Formula (Ib) as follows: wherein Y, Z, and n are defined herein; and wherein Yb and Zb are as defined herein.

Microwave-assisted syntheses of 2-phenylbenzothiazoles

A new and easy synthetic route to 2-phenylbenzothiazoles has been achieved by direct thiation of benzoyl derivatives of aniline, various substituted anilines, and 1-naphthylamine under microwave irradiation. The oxidative cyclization using elemental sulfur in the presence of a catalytic amount of iodine is inexpensive and worked well for a number of anilides. Copyright Taylor & Francis Group, LLC.