116611-42-8

Basic information

• Product Name: L-Cysteine, N-[(1,1-dimethylethoxy)carbonyl]-S-phenyl-, methyl ester
• CAS NO: 116611-42-8
• Molecular Formula: C15H21NO4S
• Molecular Weight: 311.402
• Mol File: 116611-42-8.mol
• Article Data: 11

Chemical Properties

• CAS DataBase Reference: L-Cysteine, N-[(1,1-dimethylethoxy)carbonyl]-S-phenyl-, methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: L-Cysteine, N-[(1,1-dimethylethoxy)carbonyl]-S-phenyl-, methyl ester(116611-42-8)
• EPA Substance Registry System: L-Cysteine, N-[(1,1-dimethylethoxy)carbonyl]-S-phenyl-, methyl ester(116611-42-8)

Safety Data

• Hazardous Substances Data: 116611-42-8(Hazardous Substances Data)

Upstream product

• 930-69-8 sodium thiophenolate 
• 56926-94-4 methyl (2S)-2-[N-(t-butoxycarbonyl)amino]-3-(4-methylbenzenesulfonyl)-oxypropionate 
• 2766-43-0 N-tert-butyloxycarbonyl-L-serine methyl ester 
• 882-33-7 diphenyldisulfane 
• 187035-34-3 (S)-2-tert-butoxycarbonylamino-3-methanesulfonyloxypropionic acid methyl ester 
• 108-98-5 thiophenol 
• 124-63-0 methanesulfonyl chloride 
• 34017-29-3 (R)-2-amino-3-phenylsulfanyl-propionic acid methyl ester hydrochloride 
• 24424-99-5 di-tert-butyl dicarbonate 
• 175844-11-8 methyl (2R)-2-[(tert-butoxycarbonyl)amino]-3-bromopropionate 
• 95715-85-8 2-(tert-butoxycarbonylamino)-3-hydroxypropionic acid methyl ester 
• 1621706-89-5 methyl (4R)-3-(tert-butyloxycarbonyl)-2,2-dioxo-1,2,3-oxathiazolidine-4-carboxylate 
• 67-56-1 methanol 
• 59524-02-6 (R)-benzyl 2-((tert-butoxycarbonyl)amino)-3-hydroxypropanoate 

Downstream Products

• 406233-60-1 ((R)-1-formyl-2-phenylsulfanylethyl)carbamic acid tert-butyl ester 
• 1043499-68-8 (R)-S-benzenesulfonyl-2-tert-butoxycarbonylamino-propionic acid methyl ester 
• 1619923-36-2 (R)-3-(1-(3-(4-(N-(4-(4-(3-(2-(4-chlorophenyl)-1-isopropyl-5-methyl-4-(methylsulfonyl)-1H-pyrrol-3-yl)-5-fluorophenyl)piperazin-1-yl)phenyl)sulfamoyl)-2-(trifluoromethylsulfonyl)phenylamino)-4-(phenylthio)butyl)piperidine-4-carbonyloxy)propylphosphonic acid 
• 116611-51-9 [(R)-2-Benzenesulfonyl-3-phenyl-1-(tetrahydro-pyran-2-yloxymethyl)-propyl]-carbamic acid tert-butyl ester 
• 116611-53-1 [(R)-2-Benzenesulfonyl-1-(tetrahydro-pyran-2-yloxymethyl)-pentyl]-carbamic acid tert-butyl ester 
• 116611-52-0 [(R)-2-Benzenesulfonyl-1-(tetrahydro-pyran-2-yloxymethyl)-butyl]-carbamic acid tert-butyl ester 
• 116611-60-0 ((R)-2-Benzenesulfonyl-1-hydroxymethyl-3-phenyl-propyl)-carbamic acid tert-butyl ester 
• 116611-62-2 ((R)-2-Benzenesulfonyl-1-hydroxymethyl-pentyl)-carbamic acid tert-butyl ester 
• 116611-61-1 ((R)-2-Benzenesulfonyl-1-hydroxymethyl-butyl)-carbamic acid tert-butyl ester 
• 116611-44-0 ((R)-2-benzenesulfonyl-1-hydroxymethyl-ethyl)carbamic acid tert-butyl ester 
• 116611-54-2 (1S-hydroxymethyl-3-phenylpropyl)carbamic acid tert-butyl ester 
• 116611-57-5 tert-butyl [(1S)-1-(hydroxymethyl)butyl]carbamate 
• 116640-17-6 tert-butyl [(1S)-1-(hydroxymethyl)pentyl]carbamate 
• 116611-45-1 (2R)-2-t-butoxycarbonylamino-3-phenylsulfonyl-1-(2-tetrahydropyranyloxy)propane 

Relevant articles and documents

Process for preparing sulfonamide compounds

The invention relates to a process for preparing sulfonamide compounds. The sulfonamide compound is an inhibitor of Bcl-2/Bcl-xL and is prepared from a compound (3R)-1-(3-(4-(4-(4-(3-(2-(4-chlorphenyl)-1-isopropyl-4-methylsulfonyl-5-methyl-1H-pyrrole-3-yl

Metal-free S-arylation of cysteine using arenediazonium salts

A mild chemoselective method for S-arylation of cysteine has been developed in an open-flask procedure under metal-free conditions using arenediazonium salts in methanol.

Zn in ionic liquid: An efficient reaction media for the synthesis of diorganyl chalcogenides and chalcogenoesters

A straightforward and efficient methodology is described to synthesize structurally diverse diorganyl selenides, sulfides, seleno- and thioesters by using commercially available Zn dust in ionic liquid. Excellent yields were achieved under neutral conditions at room temperature in a short time. The solvent/ionic liquid is reusable and exhibited higher performance as compared with organic solvents.