148469-28-7

Basic information

• Product Name: (R)-<2-Carboxy-2-<(methoxycarbonyl)amino>ethyl>triphenylphosphonium Chloride
• CAS NO: 148469-28-7
• Molecular Weight: 443.867
• Mol File: 148469-28-7.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (R)-<2-Carboxy-2-<(methoxycarbonyl)amino>ethyl>triphenylphosphonium Chloride(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-<2-Carboxy-2-<(methoxycarbonyl)amino>ethyl>triphenylphosphonium Chloride(148469-28-7)
• EPA Substance Registry System: (R)-<2-Carboxy-2-<(methoxycarbonyl)amino>ethyl>triphenylphosphonium Chloride(148469-28-7)

Safety Data

• Hazardous Substances Data: 148469-28-7(Hazardous Substances Data)

Upstream product

• 96854-28-3 (R)-<2-(Benzyloxycarbonyl)-2-<(methoxycarbonyl)amino>ethyl>triphenylphosphonium Iodide 
• 136978-32-0 (S)-N-(Methoxycarbonyl)-O-(p-toluenesulfonyl)serine Benzyl Ester 
• 99259-17-3 (S)-N-(Methoxycarbonyl)serine Benzyl Ester 
• 603-35-0 triphenylphosphine 
• 99259-18-4 (R)-3-Iodo-2-<(methoxycarbonyl)amino>propanoic Acid Benzyl Ester 
• 96854-33-0 ((R)-2-Benzyloxycarbonyl-2-methoxycarbonylamino-ethyl)-triphenyl-phosphonium; chloride 

Downstream Products

• 96854-31-8 -4-<1-Benzyl-4,9-dihydro-4,6-dimethyl-9-oxo-1H-imidazo<1,2-a>purin-7-yl>-2-<(methoxycarbonyl)amino>-3-butenoic Acid Methyl Ester 
• 136978-28-4 (S)-(E)-(1-benzyl-4,6-dimethyl-9-oxo-4,9-dihydro-1H-imidazo<1,2-a>purin-7-yl)-2-<(methoxycarbonyl)amino>but-3-enoic acid 
• 136978-29-5 1-Benzyl-6-[(E)-2-(1-benzyl-4,6-dimethyl-9-oxo-4,9-dihydro-1H-imidazo[1,2-a]purin-7-yl)-vinyl]-4-methyl-9-oxo-4,9-dihydro-1H-imidazo[1,2-a]purine-7-carbaldehyde 
• 136978-25-1 -2-(methoxycarbonyl)amino-4-phenyl-3-butenoic acid 
• 128885-39-2 (S)-4-Hydroxy-2-methoxycarbonylamino-4-phenyl-butyric acid 

Relevant articles and documents

Synthesis and absolute configuration of wybutine, the fluorescent minor base from phenylalanine transfer ribonucleic acids

The phosphonium chloride 6 having an optically active amino acid moiety was synthesized from (S)-serine benzyl ester tosylate (2b) through a six-step route. The utility of 6 as a reagent for the Wittig reaction was exemplified in the olefination with benz