54788-34-0

Basic information

• Product Name: Carbamic acid, [1-(diethoxyphosphinyl)ethyl]-, phenylmethyl ester
• CAS NO: 54788-34-0
• Molecular Formula: C14H22NO5P
• Molecular Weight: 315.306
• Mol File: 54788-34-0.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Carbamic acid, [1-(diethoxyphosphinyl)ethyl]-, phenylmethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Carbamic acid, [1-(diethoxyphosphinyl)ethyl]-, phenylmethyl ester(54788-34-0)
• EPA Substance Registry System: Carbamic acid, [1-(diethoxyphosphinyl)ethyl]-, phenylmethyl ester(54788-34-0)

Safety Data

• Hazardous Substances Data: 54788-34-0(Hazardous Substances Data)

Upstream product

• 762-04-9 phosphonic acid diethyl ester 
• 30094-28-1 2-(diethylphosphono)propionic acid 
• 100-51-6 benzyl alcohol 
• 4132-86-9 N-benzyloxycarbonylalanine 
• 621-84-1 O-benzyl carbamate 
• 75-07-0 acetaldehyde 
• 64-17-5 ethanol 
• 65164-80-9 diphenyl 1-(phenylmethoxycarbonylamino)ethyl phosphonate 
• 60668-25-9 N-benzyloxycarbonyl-α-aminoethylphosphonic acid 
• 122-51-0 orthoformic acid triethyl ester 

Downstream Products

• 133981-30-3 C₂₂H₂₉N₂O₆P 
• 130568-28-4 N-(Benzyloxycarbonylamino ethyl ethoxyphosphinyl) glycine ethyl ester 
• 130568-27-3 N-(Benzyloxycarbonylamino ethyl ethoxyphosphinyl)-alanine methyl ester 
• 289658-75-9 Diethyl-N-(benzyloxycarbonyl)-L-alanyl-(2-decarboxy-DL-alanin-2-yl)phosphonat 
• 54788-36-2 diethyl N-benzyloxycarbonyl-D-alanyl-1-aminoethylphosphonate 
• 54788-36-2 diethyl N-(N-carbobenzyloxy-DL-alanyl)-1-aminoethylphosphonate 
• 146304-04-3 [1-(2-Benzyloxycarbonylamino-acetylamino)-ethyl]-phosphonic acid diethyl ester 
• 81070-98-6 diethyl N-carbobenzyloxy-N-methyl-1-aminoethylphosphonate 
• 61937-75-5 N-benzyloxycarbonyl-1-aminoethanephosphonic acid ethyl monoester 
• 60668-25-9 N-benzyloxycarbonyl-α-aminoethylphosphonic acid 
• 54788-35-1 diethyl 1-aminoethylphosphonate 
• 6323-97-3 1-aminoethanephosphonic acid 

Relevant articles and documents

STUDIES ON ORGANOPHOSPHORUS COMPOUNDS. 65, A FACILE SYNTHETIC ROUTE TO PHOSPHONOPEPTIDES

A direct procedure for the preparation of phosphonopeptides, containing either a N- or C-terminal phosphonic acid residue, is described.This method is based on a three component condensation reaction leading to diethyl 1-(N-carbobenzyloxyamino)-alkylphosp

CONVERSION OF AMINO ACIDS AND DIPEPTIDES INTO THEIR PHOSPHONIC ANALOGS; Aminoalkylphosphonic acids and peptides II.

Acylamino carboxylic acids were degradated by the Hunsdiecker-reaction; the bromo-derivatives were reacted with NaPO(OC2H5)2.Aminophosphonic acids were obtained by acidic hydrolysis, and half-blocked derivatives by the selective removal of masking substituents.Two phosphonopeptides were also prepared by this route.

Synthesis and antimicrobial evaluation of N D alanyl 1 aminoethylphosphonic acid

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