615264-92-1

Basic information

• Product Name: (R)-1-benzyloxycarbonylamino-1-phenylmethylphosphonic acid
• Synonyms: (R)-1-benzyloxycarbonylamino-1-phenylmethylphosphonic acid
• CAS NO: 615264-92-1
• Molecular Weight: 321.269
• Mol File: 615264-92-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (R)-1-benzyloxycarbonylamino-1-phenylmethylphosphonic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-1-benzyloxycarbonylamino-1-phenylmethylphosphonic acid(615264-92-1)
• EPA Substance Registry System: (R)-1-benzyloxycarbonylamino-1-phenylmethylphosphonic acid(615264-92-1)

Safety Data

• Hazardous Substances Data: 615264-92-1(Hazardous Substances Data)

Upstream product

• 688047-38-3 (R)-bis(2-nitrobenzyl)((benzylamino)(phenyl)methyl) phosphonate 
• 100-52-7 benzaldehyde 
• 621-84-1 O-benzyl carbamate 
• 501-53-1 benzyl chloroformate 
• 37714-05-9 (R)-1-amino-1-phenylmethylphosphonic acid 
• 53558-70-6 α-(N-benzyloxycarbonyl)amino-benzylphosphonic acid 
• 27845-50-7 (E)-N-benzylidenebenzylamine 

Relevant articles and documents

Straightforward synthesis of depsiphosphonopeptides via Mannich-type multicomponent condensation

A straightforward method for the synthesis of depsiphosphonopeptides via a Mannich-type multicomponent condensation of simple starting materials, such as benzyl carbamate, aldehydes, and 1-carbethoxyalkyl phosphorodichloridites, was developed. Compared to

High-performance liquid chromatographic enantiomer separation and determination of absolute configurations of phosphinic acid analogues of dipeptides and their α-aminophosphinic acid precursors

The enantiomers of N-benzyloxycarbonyl-phosphinic pseudodipeptides and their N-benzyloxycarbonyl-α-aminophosphinic acid precursors as well as various other structural analogues were separated on a set of cinchona alkaloid-derived chiral anion-exchangers b