135348-32-2

Basic information

• Product Name: [Benzyloxycarbonylamino-(4-chloro-phenyl)-methyl]-phosphonic acid monoethyl ester
• CAS NO: 135348-32-2
• Molecular Weight: 383.768
• Mol File: 135348-32-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: [Benzyloxycarbonylamino-(4-chloro-phenyl)-methyl]-phosphonic acid monoethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: [Benzyloxycarbonylamino-(4-chloro-phenyl)-methyl]-phosphonic acid monoethyl ester(135348-32-2)
• EPA Substance Registry System: [Benzyloxycarbonylamino-(4-chloro-phenyl)-methyl]-phosphonic acid monoethyl ester(135348-32-2)

Safety Data

• Hazardous Substances Data: 135348-32-2(Hazardous Substances Data)

Upstream product

• 64-17-5 ethanol 
• 621-84-1 O-benzyl carbamate 
• 104-88-1 4-chlorobenzaldehyde 
• 1498-42-6 phosphorodichloridous acid ethyl ester 

Downstream Products

• 146304-18-9 C₂₁H₂₆ClN₂O₆P 

Relevant articles and documents

A modified method for synthesis of alkyl hydrogen α-(benzyloxycarbonylamino)-benzylphosphonates

A series of alkyl hydrogen α-(benzyloxycarbonylamino)benzylphosphosphonates are prepared from benzyl carbamate, substituted benzaldehydes and alkoxydichlorophosphine in acetyl chloride and subsequent hydrolysis. Compared with the previous methods, the reaction avoids producing the corresponding diesters and thus improves the yields of the products.

Studies on Organophosphorus Compounds; XLI. A Convenient Synthesis of Alkyl Hydrogen α-(Benzyloxycarbonylamino)benzylphosphonates

Alkyl hydrogen α-(benzyloxycarbonylamino)benzylphosphonates are prepared from substituted benzaldehydes, benzyl carbamate, and phosphorus(III) chloride in acetic acid containing thionyl chloride and subsequent alcoholysis.The reactions proceed smoothly at