96854-24-9

Basic information

• Product Name: N-(Methoxycarbonyl)-L-serine Methyl Ester
• Synonyms: N-(Methoxycarbonyl)-L-serine Methyl Ester;ZJGPAXKSMSICGP-BYPYZUCNSA-N
• CAS NO: 96854-24-9
• Molecular Formula: C₆H₁₁NO₅
• Molecular Weight: 177.15524
• Product Categories: Aliphatics, Amino Acids & Derivatives
• Mol File: 96854-24-9.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: N-(Methoxycarbonyl)-L-serine Methyl Ester(CAS DataBase Reference)
• NIST Chemistry Reference: N-(Methoxycarbonyl)-L-serine Methyl Ester(96854-24-9)
• EPA Substance Registry System: N-(Methoxycarbonyl)-L-serine Methyl Ester(96854-24-9)

Safety Data

• Hazardous Substances Data: 96854-24-9(Hazardous Substances Data)

Usage

Uses

N-(Methoxycarbonyl)-L-serine Methyl Ester, can be used in the synthesis of Tn antigen (GalNAc-α-O-Ser), which has a great biological properties.

Upstream product

• 2788-84-3 (S)-serine methyl ester 
• 79-22-1 methyl chloroformate 
• 2104-89-4 D-serine methyl ester 
• 5680-80-8 methyl (2S)-2-amino-3-hydroxypropanoate hydrochloride 
• 186581-53-3 diazomethane 

Downstream Products

• 96854-25-0 (S)-N-(Methoxycarbonyl)-O-(p-toluenesulfonyl)serine Methyl Ester 
• 147671-72-5 [(S)-1-(tert-Butyl-dimethyl-silanyloxymethyl)-2-(tert-butyl-diphenyl-silanyloxy)-ethyl]-carbamic acid methyl ester 
• 141943-22-8 (R)-4-(2,3-Dimethoxy-phenyl)-2-methoxycarbonylamino-butyric acid 
• 141943-20-6 (R)-2,2-Dimethyl-4-((S)-3,3,3-trifluoro-2-methoxy-2-phenyl-propionyloxymethyl)-oxazolidine-3-carboxylic acid methyl ester 
• 141943-22-8 (S)-4-(2,3-Dimethoxy-phenyl)-2-methoxycarbonylamino-butyric acid 
• 96854-27-2 (R)-<2-(Methoxycarbonyl)-2-<(methoxycarbonyl)amino>ethyl>triphenylphosphonium Iodide 

Relevant articles and documents

Process for a phenylthiobutyl-isoquinoline and intermediates therefor

The present invention relates to a new method for making compounds of formula and intermediates for making compounds of formual II. The compounds of this invention are useful intermediates for the manufacture of pharmacologically active compounds suitable

Enantiospecific synthesis of R- and S-5,6-dihydroxy-2-(N,N-di-n-propylamino)tetralins from serine

The first enantiospecific synthesis of 5,6-dihydroxy-2-(N,N-di-n-propylamino)tetralin [5,6-(HO)2DPAT] is reported. Starting from D- or L-serine either enantiomer is readily available in high optical purity.