95406-98-7

Basic information

• Product Name: D-Cysteine, S-methyl-N-[(phenylmethoxy)carbonyl]-
• CAS NO: 95406-98-7
• Molecular Formula: C12H15NO4S
• Molecular Weight: 269.321
• Mol File: 95406-98-7.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: D-Cysteine, S-methyl-N-[(phenylmethoxy)carbonyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: D-Cysteine, S-methyl-N-[(phenylmethoxy)carbonyl]-(95406-98-7)
• EPA Substance Registry System: D-Cysteine, S-methyl-N-[(phenylmethoxy)carbonyl]-(95406-98-7)

Safety Data

• Hazardous Substances Data: 95406-98-7(Hazardous Substances Data)

Upstream product

• 921-01-7 D-cysteine 
• 501-53-1 benzyl chloroformate 
• 74-88-4 methyl iodide 
• 52-90-4 L-Cysteine 
• 77-78-1 dimethyl sulfate 
• 1187-84-4 S-methyl-L-cysteine 
• 95406-97-6 N-(benzyloxycarbonyl)-S-methyl-D,L-cysteine 

Downstream Products

• 133444-83-4 (R)-benzyl (1-(methylthio)-3-oxopropan-2-yl)carbamate 
• 1276690-62-0 C₁₄H₁₉NO₄S 
• 66877-28-9 [1-((S)-2-Methyl-1-methylcarbamoyl-propylcarbamoyl)-vinyl]-carbamic acid benzyl ester 
• 63095-89-6 [1-((S)-1-Methylcarbamoyl-ethylcarbamoyl)-vinyl]-carbamic acid benzyl ester 
• 95407-03-7 N-(benzyloxycarbonyl)-S-methyl-D-cysteinol S-oxide 
• 95407-02-6 N-(benzyloxycarbonyl)-S-methyl-D-cysteinol S-oxide 
• 95463-96-0 N-(benzyloxycarbonyl)-O-(tetrahydropyranyl)-S-methyl-D-cysteinol S-oxide 
• 95407-10-6 (R_S)-N-(benzyloxycarbonyl)-O-(methoxymethyl)-S-methyl-D-cysteinol S-oxide 
• 95407-09-3 (S_S)-N-(benzyloxycarbonyl)-O-(methoxymethyl)-S-methyl-D-cysteinol S-oxide 
• 95407-08-2 N-(benzyloxycarbonyl)-O-(methoxymethyl)-S-methyl-D-cysteinol 
• 95407-01-5 N-(benzyloxycarbonyl)-S-methyl-D-cysteinol 

Relevant articles and documents

Synthesis and activity of pyrimidinylpropenamide antibiotics: The alkyl analogues of sparsomycin

Facile syntheses of sparsomycin (3) and its four analogues (4-7) based on diastereoselective oxidation of sulfide, sulfenylation, and coupling of 6-methyluracylacryllic acid with monooxodithioacetal amine, are described. Studies on the biological activity of morphological reversion on src ts-NRK cells were also carried out.

α-Amino Aldehydes as Readily Available Chiral Aldehydes for Rh-Catalyzed Alkyne Hydroacylation

Readily available α-amino aldehydes, incorporating a methylthiomethyl (MTM) protecting group on nitrogen, are shown to be efficient substrates in Rh-catalyzed alkyne hydroacylation reactions. The reactions are performed under mild conditions, employing a small-bite-angle bis-phosphine ligand, allowing for good functional group tolerance with high stereospecificity. Amino aldehydes derived from glycine, alanine, valine, leucine, phenylalanine, isoleucine, serine, tryptophan, methionine, and cysteine were successfully employed, as was an enantiomerically enriched α-OMTM-aldehyde derived from phenyllactic acid. The synthetic utility of the α-amino enone products is demonstrated in a short enantioselective synthesis of the natural product sphingosine.

Total synthesis of (+)-sparsomycin. Approaches using cysteine and serine inversion

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