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S-Benzyl-L-cysteine

Base Information
  • Chemical Name:S-Benzyl-L-cysteine
  • CAS No.:25988-62-9
  • Molecular Formula:C10H13NO2S
  • Molecular Weight:211.285
  • Hs Code.:
  • European Community (EC) Number:221-273-4
  • UNII:9VRE13M548
  • DSSTox Substance ID:DTXSID60180650
  • Nikkaji Number:J62.817D
  • Wikidata:Q27075094
  • Pharos Ligand ID:FC6GK5XFMM5P
  • ChEMBL ID:CHEMBL63130
S-Benzyl-L-cysteine

Synonyms:S-benzyl-L-cysteine;S-benzylcysteine;S-benzylcysteine, 2-13C-labeled

Suppliers and Price of S-Benzyl-L-cysteine
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
Total 4 raw suppliers
Chemical Property of S-Benzyl-L-cysteine
Chemical Property:
  • Appearance/Colour:solid 
  • Storage Temp.:−20°C 
  • XLogP3:-1.2
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:5
  • Exact Mass:211.06669983
  • Heavy Atom Count:14
  • Complexity:181
Purity/Quality:

98%min *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

Total 1 MSDS from other Authors

Useful:
  • Canonical SMILES:C1=CC=C(C=C1)CSCC(C(=O)O)N
  • Isomeric SMILES:C1=CC=C(C=C1)CSC[C@@H](C(=O)O)N
Technology Process of S-Benzyl-L-cysteine

There total 54 articles about S-Benzyl-L-cysteine which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With sodium hydroxide; In ethanol;
DOI:10.1039/b306124h DOI:10.1039/b404205k
Guidance literature:
With N,N,N',N'-tetramethylguanidine; In tetrahydrofuran; at 50 ℃; for 1h; Inert atmosphere;
DOI:10.1016/j.tetlet.2010.08.097
Guidance literature:
With potassium phosphate buffer; pyridoxal 5'-phosphate; at 30 ℃; for 12h; α2β2 complex of tryptophan synthase from Escherichia coli;
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