1570135-34-0

Basic information

• Product Name: 2-chloro-N-(2-((2-(4,5-dihydrooxazol-2-yl)phenyl)carbamoyl)phenyl)-6-nitrobenzamide
• Synonyms: 2-chloro-N-(2-((2-(4,5-dihydrooxazol-2-yl)phenyl)carbamoyl)phenyl)-6-nitrobenzamide
• CAS NO: 1570135-34-0
• Molecular Weight: 464.865
• Mol File: 1570135-34-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2-chloro-N-(2-((2-(4,5-dihydrooxazol-2-yl)phenyl)carbamoyl)phenyl)-6-nitrobenzamide(CAS DataBase Reference)
• NIST Chemistry Reference: 2-chloro-N-(2-((2-(4,5-dihydrooxazol-2-yl)phenyl)carbamoyl)phenyl)-6-nitrobenzamide(1570135-34-0)
• EPA Substance Registry System: 2-chloro-N-(2-((2-(4,5-dihydrooxazol-2-yl)phenyl)carbamoyl)phenyl)-6-nitrobenzamide(1570135-34-0)

Safety Data

• Hazardous Substances Data: 1570135-34-0(Hazardous Substances Data)

Upstream product

• 1570134-48-3 N-(2-(4,5-dihydrooxazol-2-yl)phenyl)benzamide 
• 107485-64-3 2-chloro-6-nitro-benzoic acid amide 

Relevant articles and documents

Cu(II)-mediated C-H amidation and amination of arenes: Exceptional compatibility with heterocycles

A Cu(OAc)2-mediated C-H amidation and amination of arenes and heteroarenes has been developed using a readily removable directing group. A wide range of sulfonamides, amides, and anilines function as amine donors in this reaction. Heterocycles present in both reactants are tolerated, making this a broadly applicable method for the synthesis of a family of inhibitors including 2-benzamidobenzoic acids and N-phenylaminobenzoates.