155104-20-4

Basic information

• Product Name: N-chloroacetyl-5-bromoanthranilic acid
• Synonyms: N-chloroacetyl-5-bromoanthranilic acid
• CAS NO: 155104-20-4
• Molecular Weight: 292.516
• Mol File: 155104-20-4.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: N-chloroacetyl-5-bromoanthranilic acid(CAS DataBase Reference)
• NIST Chemistry Reference: N-chloroacetyl-5-bromoanthranilic acid(155104-20-4)
• EPA Substance Registry System: N-chloroacetyl-5-bromoanthranilic acid(155104-20-4)

Safety Data

• Hazardous Substances Data: 155104-20-4(Hazardous Substances Data)

Upstream product

• 5794-88-7 5-Bromo-2-aminobenzoic acid 
• 79-04-9 chloroacetyl chloride 
• 14422-49-2 2-chloroacetamidobenzoic acid 

Downstream Products

• 155104-09-9 6-bromo-2-(chloromethyl)-3-<3'-hydroxy-4'-(methoxycarbonyl)phenyl>-4(3H)-quinazolinone 
• 179912-40-4 5-bromo-N-cyanoacetylanthranilic acid 
• 195393-30-7 5-bromo-2-(2-phenylamino-acetylamino)-benzoic acid 
• 155104-16-8 6-bromo-2-(1-carboxyethylthiomethyl)-3-<3'-hydroxy-4'-(methoxycarbonyl)phenyl>-4(3H)-quinazolinone 
• 155104-14-6 6-bromo-2-(2-carboxyethylthiomethyl)-3-<3'-hydroxy-4'-(methoxycarbonyl)phenyl>-4(3H)-quinazolinone 
• 155104-15-7 6-bromo-2-(1-carboxyethylthiomethyl)-3-<4'-(ethoxycarbonyl)phenyl>-4(3H)-quinazolinone 
• 155104-12-4 6-bromo-2-(carboxymethylthiomethyl)-3-<3'-hydroxy-4'-(methoxycarbonyl)phenyl>-4(3H)-quinazolinone 
• 155104-13-5 6-bromo-2-(2-carboxyethylthiomethyl)-3-<4-(ethoxycarbonyl)phenyl>-4(3H)-quinazolinone 
• 155104-11-3 6-bromo-2-(carboxymethylthiomethyl)-3-<4'-(ethoxycarbonyl)phenyl>-4(3H)-quinazolinone 
• 177167-00-9 6-bromo-2-chloromethyl-3-o-tolyl-3H-quinazolin-4-one 

Relevant articles and documents

Synthesis of 3-[4′-(p-chlorophenyl)-thiazol-2′-yl]-2-[(substituted azetidinone/thiazolidinone)-aminomethyl]-6-bromoquinazolin-4-ones as anti-inflammatory agent

N-Chloroacetyl-5-bromoanthranilic acid (1), 3-[4′-(p-chlorophenyl)-thiazol-2′-yl]-2-chloromethyl-6-bromoquinazolin-4-one (2), 3-[4′-(p-chlorophenyl)-thiazol-2′-yl]-2-hydrazinomethyl-6-bromoquinazolin-4-one (3), 3-[4′-(p-chlorophenyl)-thiazol-2′-yl]-2-subs

The Vilsmeier cyclisation of azides: A novel route towards the synthesis of imidazo[1,2-a]quinazoline-1,5-diones

Imidazo[1,2-a]quinazoline-1,5-diones 2a-d have been prepared in one pot from 2-azido-N-(2-carboxyaryl)acetamides 1a-d.

Synthesis and biological activities of 6-bromo-2,3-disubstituted-4-(3H)-quinazolinones

The title compounds 6-bromo-2,3-disubstituted-4(3H)-quinazolinones (5a-11a and 6b-8b) have been synthesized for evaluation as potential sedative-hypnotic, anti-convulsant and antiinflammatory agents.Compound 5a has been synthesized by condensing 6-bromo-2