39801-36-0

Basic information

• Product Name: L-Cysteine, S-(phenylmethyl)-, phenylmethyl ester
• CAS NO: 39801-36-0
• Molecular Formula: C17H19NO2S
• Molecular Weight: 301.409
• Mol File: 39801-36-0.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: L-Cysteine, S-(phenylmethyl)-, phenylmethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: L-Cysteine, S-(phenylmethyl)-, phenylmethyl ester(39801-36-0)
• EPA Substance Registry System: L-Cysteine, S-(phenylmethyl)-, phenylmethyl ester(39801-36-0)

Safety Data

• Hazardous Substances Data: 39801-36-0(Hazardous Substances Data)

Upstream product

• 100-53-8 phenylmethanethiol 
• 100-51-6 benzyl alcohol 
• 3054-01-1 S-benzyl-L-cysteine 

Downstream Products

• 4191-62-2 S-benzyl-N-(N-benzyloxycarbonyl-glycyl)-L-cysteine benzyl ester 
• 116928-49-5 S-benzyl-N-(S-benzyl-N-benzyloxycarbonyl-L-cysteinyl)-D-cysteine benzyl ester 
• 7669-86-5 S-benzyl-N-(S-benzyl-L-cysteinyl)-L-cysteine 
• 122804-10-8 N²-(toluene-4-sulfonyl)-L-glutaminyl=>L-isoasparaginyl=>S-benzyl-L-cysteine benzyl ester 
• 806636-05-5 S-benzyl-N-L-isoasparaginyl-L-cysteine benzyl ester 
• 104339-31-3 N-benzyloxycarbonyl-glycyl=>glycyl=>glycyl=>glycyl=>S-benzyl-L-cysteine benzyl ester 
• 102679-68-5 S-benzyl-N-(N-glycyl-glycyl)-L-cysteine benzyl ester 
• 97735-60-9 S-benzyl-N-{N-[N-(S-benzyl-N-benzyloxycarbonyl-L-cysteinyl)-glycyl]-glycyl}-L-cysteine benzyl ester 
• 34100-99-7 S-benzyl-N-{N-[N-(N-benzyloxycarbonyl-glycyl)-glycyl]-glycyl}-L-cysteine benzyl ester 
• 116928-49-5 S-benzyl-N-(S-benzyl-N-benzyloxycarbonyl-L-cysteinyl)-L-cysteine benzyl ester 
• 103209-68-3 S-benzyl-N-[N-(N-benzyloxycarbonyl-glycyl)-glycyl]-L-cysteine benzyl ester 
• 116281-72-2 N²-(toluene-4-sulfonyl)-L-glutaminyl=>S-benzyl-L-cysteinyl=>S-benzyl-L-cysteine benzyl ester 
• 116280-95-6 N²-(toluene-4-sulfonyl)-L-glutaminyl=>L-asparaginyl=>S-benzyl-L-cysteine benzyl ester 
• 19898-05-6 S-benzyl-N-(N²-benzyloxycarbonyl-L-asparaginyl)-L-cysteine benzyl ester 

Relevant articles and documents

Beta-replacement reaction of serine-O-carbonate derivatives with thiols catalyzed by a pyridoxal model having an ionophore side-chain.

Serine-O-carbonate derivatives, including peptides having a serine-O-carbonate residue at the N-terminal position, are catalytically transformed into S-substituted cysteine derivatives employing the pyridoxal model having an ionophore function in the pres

Artificial model for cystathionine β-synthase: Construction of a catalytic cycle with a pyridoxal model compound having an ionophore function

Catalytic transformation of serine-O-carbonate to S-aryl cysteine derivatives was successfully achieved in the presence of Li+ by the use of a pyridoxal model compound having an ionophore function, which is the first example mimicking cystathionine β-synthase, artificially.