84446-17-3

Basic information

• Product Name: 3-(2'-bromobenzoyl)amino-2-chloropyridine
• Synonyms: 3-(2'-bromobenzoyl)amino-2-chloropyridine
• CAS NO: 84446-17-3
• Molecular Formula: C₁₂H₈BrClN₂O
• Molecular Weight: 312
• Mol File: 84446-17-3.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 3-(2'-bromobenzoyl)amino-2-chloropyridine(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(2'-bromobenzoyl)amino-2-chloropyridine(84446-17-3)
• EPA Substance Registry System: 3-(2'-bromobenzoyl)amino-2-chloropyridine(84446-17-3)

Safety Data

• Hazardous Substances Data: 84446-17-3(Hazardous Substances Data)

Upstream product

• 6298-19-7 2-chloro-3-aminopyridine 
• 7154-66-7 2-bromobenzoic acid chloride 

Downstream Products

• 67588-13-0 2-(2'-bromophenyl)oxazolo<5,4-b>pyridine 
• 88369-31-7 3-amino-1-benzylpyrid-2-one 
• 88369-32-8 3-amino-1-benzylpyrid-2-one 
• 28797-61-7 pirenzepine 
• 79276-55-4 5,11-dihydro-11-<(2'-methylimidazo-1'-yl)-acetyl>-6H-pyrido<2,3-b><1,4>benzodiazepin-6-one 
• 79276-54-3 5,11-dihydro-11-<(imidazo-1'-yl)-acetyl>-6H-pyrido<2,3-b><1,4>benzodiazepin-6-one 
• 84446-20-8 1-oxo-11,2'-(4''-methylpiperazin-1''-yl)acetyl-5,11-dihydro-6H-pyrido<2,3-b><1,4>benzodiazepin-6-one 
• 84446-11-7 1-oxo-5,11-dihydro-11-imidazol-1'-ylacetyl-6H-pyrido<2,3-b><1,4>benzodiazepin-6-one 
• 88369-80-6 3-amino-2-(2'-carboxyphenyl-2-hydroxy)aminopyridine N-oxide 
• 88369-79-3 3-amino-2-(2'-carboxyphenyl)aminopyridine N-oxide 
• 88369-72-6 3-(2'-aminobenzoyl)amino-2-chloropyridine 1-oxide 
• 88369-73-7 3-(2'-benzylaminobenzoyl)amino-2-chloropyridine 
• 88369-77-1 3-<(2''-hydroxyethyl)-2'-aminobenzoyl>amino-2-chloropyridine 
• 88369-78-2 1-<2'-(2''-chloropyridylamido-3'')carboxy>phenyloxy-2-<2'-(2''-chloropyridylamido-3'')carboxy>phenylaminoethane 

Relevant articles and documents

A Pd-catalyzed direct entry to 11-substituted 6H-isoindolo[2,1-a]indol-6-one derivatives as potential anticancer agents

We describe Pd-mediated one-step synthesis of 11-substituted 6H-isoindolo[2,1-a]indol-6-ones via a sequential intramolecular Heck reaction of the corresponding dihalo N-allyl substituted N-arylbenzamide derivatives. Several of these compounds showed promi