22312-63-6

Basic information

• Product Name: 2-amino-N-(3-bromophenyl)benzamide
• Synonyms: 2-amino-N-(3-bromophenyl)benzamide
• CAS NO: 22312-63-6
• Molecular Weight: 291.147
• Mol File: 22312-63-6.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2-amino-N-(3-bromophenyl)benzamide(CAS DataBase Reference)
• NIST Chemistry Reference: 2-amino-N-(3-bromophenyl)benzamide(22312-63-6)
• EPA Substance Registry System: 2-amino-N-(3-bromophenyl)benzamide(22312-63-6)

Safety Data

• Hazardous Substances Data: 22312-63-6(Hazardous Substances Data)

Usage

Chemical compound

2-amino-N-(3-bromophenyl)benzamide

Derivative

Amide of 3-bromophenyl and benzamide

Functional groups

Amino group and bromine substituent

Uses

Pharmaceutical intermediate, synthesis of medications, organic chemistry

Studies

Potential biological activities, pharmacological properties, medicinal chemistry research

Upstream product

• 118-48-9 isatoic anhydride 
• 591-19-5 m-Bromoaniline 
• 610-14-0 2-nitrobenzyl chloride 
• 552-16-9 ortho-nitrobenzoic acid 

Downstream Products

• 133040-64-9 3-(3-Bromo-phenyl)-2-[2-(1H-indol-3-yl)-ethyl]-3H-quinazolin-4-one 
• 24122-27-8 3-(3-bromophenyl)quinazolin-4(3H)-one 
• 1429192-26-6 3-(3-bromophenyl)-2-(5-methylthiophen-2-yl)-2,3-dihydroquinazolin-4(1H)-one 

Relevant articles and documents

Synthesis and biological evaluation of novel benodanil-heterocyclic carboxamide hybrids as a potential succinate dehydrogenase inhibitors

In order to discover new antifungal agents, twenty novel benodanil-heterocyclic carboxamide hybrids were designed, synthesized, and characterized by 1H NMR and HRMS. In vitro, their antifungal activities against four phytopathogenic fungi were

N-aryl(thio)anthranilic acid amide derivatives, their preparation and their use as VEGF receptor tyrosine kinase inhibitors

Described are compounds of formula (I), wherein W is O or S; X is NR8; Y is CR9R10-(CH2)n wherein R9 and R10 are independently of each other hydrogen or lower alkyl, and n is an integer of