57623-73-1

Basic information

• Product Name: Benzoyl chloride, 2-(phenylaMino)-
• Synonyms: Benzoyl chloride, 2-(phenylaMino)-
• CAS NO: 57623-73-1
• Molecular Formula: C₁₃H₁₀ClNO
• Molecular Weight: 231.6776
• EINECS: -0
• Mol File: 57623-73-1.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Benzoyl chloride, 2-(phenylaMino)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoyl chloride, 2-(phenylaMino)-(57623-73-1)
• EPA Substance Registry System: Benzoyl chloride, 2-(phenylaMino)-(57623-73-1)

Safety Data

• Hazardous Substances Data: 57623-73-1(Hazardous Substances Data)

Upstream product

• 88-67-5 2-Iodobenzoic acid 
• 62-53-3 aniline 
• 91-40-7 2-(phenylamino)benzoic acid 

Downstream Products

• 50495-81-3 N-benzoyl-N-phenyl-anthranilic acid 
• 52069-22-4 N-phenyl-anthranilic acid-anhydride 
• 578-95-0 10H-acridin-9-one 
• 91-40-7 2-(phenylamino)benzoic acid 
• 1316852-06-8 14-(3-(trifluoromethyl)phenyl)-8,13,13b,14-tetrahydroindolo[2',3':3,4]pyrido[2,1-b]quinazolin-5(7H)-one 
• 1316852-08-0 14-phenyl-1,2-dihydroquinolino[2',3':3,4]-pyrrolo[2,1-b]quinazoline-5,8(13H)-dione 
• 1316852-11-5 8-acetyloxy-14-phenyl-1,2-dihydroquinolino-[2',3':3,4]pyrrolo[2,1-b]quinazolin-5-one 
• 1316852-13-7 8-chloro-14-phenyl-1,2-dihydroquinolino-[2',3':3,4]pyrrolo[2,1-b]quinazolin-5-one 
• 1316852-15-9 8-morpholino-14-phenyl-1,2-dihydroquinol-ino[2',3':3,4]pyrrolo[2,1-b]quinazolin-5-one 
• 1415651-13-6 C₂₁H₁₈N₂O₃ 
• 1415651-18-1 C₂₃H₂₁ClN₂O₃ 
• 1415651-23-8 4-acetamidophenyl-2-[{2-(nitrooxy)ethyl}(phenyl)amino]benzoate 
• 1415651-25-0 4-acetamidophenyl-2-[{2-(nitrooxy)ethyl}(4-methylphenyl)amino]benzoate 
• 1211-19-4 2-phenylaminobenzamide 

Relevant articles and documents

Synthesis and investigation of anti-inflammatory activity of novel nitric oxide donating hybrid drugs

A small library of nitric oxide donating groups, 4-acetamidophenyl-2-[{2- (nitrooxy)ethyl}(phenyl) amino]benzoate (5a-e) possessing a variety of substituents (-H, -NO2, -CH3, -acetamidophenyl, -SO 2NH2) attached to the fourth position of phenyl ring were synthesized and evaluated for anti-inflammatory, analgesic and ulcerogenic potential. Structure-activity relationship data showed that the 2-phenylaminobenzoic acid skeleton is required for selective COX-2 inhibition. Among all compounds 4-acetamidophenyl-2-[{2-(nitrooxy)ethyl}(phenyl)amino] benzoate (5a) has shown potent anti-inflammatory activity while 4-acetamidophenyl-2-[{4-{(4-acetamidophenoxy)carbonyl} phenyl}{2-(nitrooxy) ethyl}amino]benzoate (5d) has shown potent analgesic activity compared to standard drug diclofenac.

NEW DS DNA BINDING FLUORESCENT DYES

The present invention is directed to a fluorescent dye comprising a benzothiazolium moiety and a pyrimidinium moiety connected by a mono-methine bridge, characterized in that (i) the 2-position of the pyrimidine carries a substituent which starts with a C