921198-94-9

Basic information

• Product Name: (R)-methyl 2-(N-(4,5-dichloro-2-hydroxyphenyl)-4-nitrobenzamido)-2-phenylacetate
• Synonyms: (R)-methyl 2-(N-(4,5-dichloro-2-hydroxyphenyl)-4-nitrobenzamido)-2-phenylacetate
• CAS NO: 921198-94-9
• Molecular Weight: 475.285
• Mol File: 921198-94-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (R)-methyl 2-(N-(4,5-dichloro-2-hydroxyphenyl)-4-nitrobenzamido)-2-phenylacetate(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-methyl 2-(N-(4,5-dichloro-2-hydroxyphenyl)-4-nitrobenzamido)-2-phenylacetate(921198-94-9)
• EPA Substance Registry System: (R)-methyl 2-(N-(4,5-dichloro-2-hydroxyphenyl)-4-nitrobenzamido)-2-phenylacetate(921198-94-9)

Safety Data

• Hazardous Substances Data: 921198-94-9(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 945374-90-3 N-(3,4-dichloro-6-oxocyclohexa-2,4-dienylidene)-4-nitrobenzamide 
• 103-80-0 phenylacetyl chloride 
• 921198-81-4 N-(4,5-dichloro-2-hydroxyphenyl)-4-nitrobenzamide 
• 28443-57-4 2-amino-4,5-dichlorophenol 
• 122-04-3 4-nitro-benzoyl chloride 

Relevant articles and documents

Catalytic, asymmetric inverse electron demand hetero diels-alder reactions of o-benzoquinone derivatives and ketene enolates

We present an array of [4+2] cycloaddition reactions between ketene enolates, catalytically derived from acid chlorides and cinchona alkaloid nucleophilic catalysts in the presence of stoichiometric base, and o-benzoquinone derivatives. These cycloadditio

Catalytic, asymmetric synthesis of 1,4-benzoxazinones: A remarkably enantioselective route to α-amino acid derivatives from o-benzoquinone imides

(Chemical Equation Presented) Cycloaddition of o-benzoquinone imides with chiral ketene enolates derived from cinchona alkaloid catalysts is the basis of a catalytic asymmetric synthesis of 1,4-benzoxazinones and 1,4-benzoxazines. The resulting cycloadduc