1449426-94-1

Basic information

• Product Name: methyl 2'-(phenylacetyl)[1,1'-biphenyl]-2-carboxylate
• Synonyms: methyl 2'-(phenylacetyl)[1,1'-biphenyl]-2-carboxylate
• CAS NO: 1449426-94-1
• Molecular Weight: 330.383
• Mol File: 1449426-94-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: methyl 2'-(phenylacetyl)[1,1'-biphenyl]-2-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 2'-(phenylacetyl)[1,1'-biphenyl]-2-carboxylate(1449426-94-1)
• EPA Substance Registry System: methyl 2'-(phenylacetyl)[1,1'-biphenyl]-2-carboxylate(1449426-94-1)

Safety Data

• Hazardous Substances Data: 1449426-94-1(Hazardous Substances Data)

Upstream product

• 18107-18-1 diazomethyl-trimethyl-silane 
• 103-82-2 phenylacetic acid 
• 6050-13-1 biphenyl-2,2'-dicarboxylic acid anhydride 
• 36081-66-0 2'-bromo-2-phenylacetophenone 
• 374538-03-1 2-methoxycarbonylphenylboronic acid 

Relevant articles and documents

Developments in Meyers' lactamization methodology: En route to Bi(hetero)aryl structures with defined axial chirality

Highly atroposelective Meyers' lactamization promoted by pivalic acid under microwave irradiation is reported which allows the construction of nonracemic substituted-dibenzo(di)azepine derivatives through a center to axial chirality transfer principle, controlling the otherwise configurationally labile biaryl axis. This approach provides a straightforward entry to enantioenriched analogues of biorelevant architectures.