59191-42-3

Basic information

• Product Name: 1-(N-benzyloxycarbonyl)amino-2-methylpropylphosphonic acid
• Synonyms: 1-(N-benzyloxycarbonyl)amino-2-methylpropylphosphonic acid
• CAS NO: 59191-42-3
• Molecular Weight: 287.252
• Mol File: 59191-42-3.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1-(N-benzyloxycarbonyl)amino-2-methylpropylphosphonic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(N-benzyloxycarbonyl)amino-2-methylpropylphosphonic acid(59191-42-3)
• EPA Substance Registry System: 1-(N-benzyloxycarbonyl)amino-2-methylpropylphosphonic acid(59191-42-3)

Safety Data

• Hazardous Substances Data: 59191-42-3(Hazardous Substances Data)

Upstream product

• 18108-24-2 (1-amino-2-methylpropyl)phosphonic acid 
• 501-53-1 benzyl chloroformate 
• 621-84-1 O-benzyl carbamate 
• 78-84-2 isobutyraldehyde 

Downstream Products

• 87010-57-9 (1-Benzyloxycarbonylamino-2-methyl-propyl)-phosphonic acid ethyl ester 2,2,2-trichloro-ethyl ester 
• 87010-64-8 N-benzyloxycarbonyl-1-amino-2-methylpropanephosphonic acid ethyl monoester 
• 85823-59-2 (1-Benzyloxycarbonylamino-2-methyl-propyl)-phosphonic acid monobenzhydryl ester 
• 59191-34-3 benzyl N-[1-(dimethoxyphosphoryl)-2-methylpropyl]carbamate 
• 74633-07-1 (1-Benzyloxycarbonylamino-2-methyl-propyl)-phosphonic acid dibenzhydryl ester 
• 18108-24-2 (1-amino-2-methylpropyl)phosphonic acid 
• 87010-53-5 N-benzyloxycarbonyl-1-amino-2-methylpropanephosphonic acid 2,2,2-trichloroethyl monoester 
• 61937-79-9 (1-Benzyloxycarbonylamino-2-methyl-propyl)-phosphonic acid monopropyl ester 
• 61937-78-8 Methyl (+/-)-<1-<(benzyloxycarbonyl)amino>-2-methylpropyl>phosphonic acid 

Relevant articles and documents

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An Amidoalkylation of Trivalent Phosphorus Compounds with P(O)H Functions Including Acetic Acid Solutions of PCl3, RPCl2 or R2PCl, Diesters of Phosphorous Acid and Phosphorus-III-Acids

An amidoalkylation of PCl3 or its organic derivatives in acetic acid solution takes place because equilibrium between AcOH and >P-Cl exist, leading to hydroxychlorophosphines.Those last compounds undergo an amidoalkylation like other nucleophiles.Based on these data, it was shown that an amidoalkylation reaction is usual for all phosphorus compounds with the R2P(O)H system and provides derivatives with the >N-C-P(O)R2 functions.The scope and limitation of these reactions are discussed.