1026166-78-8

Basic information

• Product Name: methanesulfonic acid ({2-[2-(3-methoxy-4-oxazol-5-yl-phenylamino)-oxazol-5-yl]-phenyl}-methyl-carbamoyl)-methyl ester
• Synonyms: methanesulfonic acid ({2-[2-(3-methoxy-4-oxazol-5-yl-phenylamino)-oxazol-5-yl]-phenyl}-methyl-carbamoyl)-methyl ester
• CAS NO: 1026166-78-8
• Molecular Weight: 498.516
• Mol File: 1026166-78-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: methanesulfonic acid ({2-[2-(3-methoxy-4-oxazol-5-yl-phenylamino)-oxazol-5-yl]-phenyl}-methyl-carbamoyl)-methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: methanesulfonic acid ({2-[2-(3-methoxy-4-oxazol-5-yl-phenylamino)-oxazol-5-yl]-phenyl}-methyl-carbamoyl)-methyl ester(1026166-78-8)
• EPA Substance Registry System: methanesulfonic acid ({2-[2-(3-methoxy-4-oxazol-5-yl-phenylamino)-oxazol-5-yl]-phenyl}-methyl-carbamoyl)-methyl ester(1026166-78-8)

Safety Data

• Hazardous Substances Data: 1026166-78-8(Hazardous Substances Data)

Upstream product

• 437655-88-4 2-(acetyloxy)-N-[2-[2-[[3-methoxy-4-(5-oxazolyl)phenyl]amino]-5-oxazolyl]phenyl]-N-methylacetamide 
• 267648-13-5 2-(acetyloxy)-N-[2-(2-azidoacetyl)phenyl]-N-methylacetamide 
• 437655-87-3 2-(acetyloxy)-N-[2-(1-ethoxyethenyl)phenyl]-N-methylacetamide 
• 437655-89-5 2-(acetyloxy)-N-[2-(2-bromoacetyl)phenyl]-N-methylacetamide 
• 437655-86-2 2-(acetyloxy)-N-(2-bromophenyl)-N-methylacetamide 
• 901335-15-7 acetic acid (2-bromo-phenylcarbamoyl)-methyl ester 
• 198821-79-3 3-methoxy-4-(1,3-oxazol-5-yl)aniline 
• 615-36-1 2-bromoaniline 
• 124-63-0 methanesulfonyl chloride 
• 437655-90-8 2-hydroxy-N-[2-[2-[[3-methoxy-4-(5-oxazolyl)phenyl]amino]-5-oxazolyl]phenyl]-N-methylacetamide 

Relevant articles and documents

A Modified Approach to 2-(N-Aryl)-1,3-oxazoles: Application to the Synthesis of the IMPDH Inhibitor BMS-337197 and Analogues

(Matrix Presented) A modified approach to the synthesis of 2-(N-aryl)-1,3-oxazoles, employing an optimized iminophosphorane/heterocumulene-mediated methodology, and its application to the synthesis of BMS-337197, a potent inhibitor of IMPDH, are described