116611-43-9

Basic information

• Product Name: (R)-2-tert-butyl carbamoyl-1-hydroxy-3-(phenylthio)propane
• Synonyms: (R)-2-tert-butyl carbamoyl-1-hydroxy-3-(phenylthio)propane
• CAS NO: 116611-43-9
• Molecular Weight: 283.392
• Mol File: 116611-43-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (R)-2-tert-butyl carbamoyl-1-hydroxy-3-(phenylthio)propane(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-2-tert-butyl carbamoyl-1-hydroxy-3-(phenylthio)propane(116611-43-9)
• EPA Substance Registry System: (R)-2-tert-butyl carbamoyl-1-hydroxy-3-(phenylthio)propane(116611-43-9)

Safety Data

• Hazardous Substances Data: 116611-43-9(Hazardous Substances Data)

Upstream product

• 116611-42-8 (R)-2-tert-butoxycarbonylamino-3-phenylsulfanylpropionic acid methyl ester 
• 2766-43-0 N-tert-butyloxycarbonyl-L-serine methyl ester 
• 56926-94-4 methyl (2S)-2-[N-(t-butoxycarbonyl)amino]-3-(4-methylbenzenesulfonyl)-oxypropionate 
• 187035-34-3 (S)-2-tert-butoxycarbonylamino-3-methanesulfonyloxypropionic acid methyl ester 
• 882-33-7 diphenyldisulfane 

Downstream Products

• 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 
• 116611-54-2 (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 
• 82732-07-8 Boc-L-homophenylalanine 
• 6404-28-0 Boc-Nle-OH 
• 53308-95-5 N-tert-butoxycarbonyl-L-norvaline 
• 116611-44-0 ((R)-2-benzenesulfonyl-1-hydroxymethyl-ethyl)carbamic acid tert-butyl ester 

Relevant articles and documents

'One-pot' synthesis and redox evaluations of chiral chalcogenocysteinol and β-bis-chalcogenoamine derivatives from l-serine methyl ester

The synthesis of a new class of chiral chalcogenocysteinols and bis-chalcogenoamines is described in this study. The compounds were prepared from commercially available l-serine using simple reactions to obtain the desired products. Additionally, the compounds were evaluated for potential antioxidant applications by cyclic voltammetry and shown to have an appropriate electrochemical oxidation potential. Density functional theory (DFT) calculations were used to better characterize the oxidative sites in the bis-chalcogenoamines, giving theoretical support to the experimental findings.

Synthesis of d-biotin from L-cystine via intramolecular [3+2}cycloaddition

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