S-(2-Thienyl)-L-cysteine

Base Information

• Chemical Name: S-(2-Thienyl)-L-cysteine
• CAS No.: 405150-23-4
• Molecular Formula: C7H9NO2S2
• Molecular Weight: 203.28200
• Hs Code.: 2934999090
• DSSTox Substance ID: DTXSID50585039
• Wikidata: Q82476832
• Mol file: 405150-23-4.mol

Synonyms:S-(2-Thienyl)-L-cysteine;405150-23-4;(2R)-2-amino-3-thiophen-2-ylsulfanylpropanoic acid;(R)-2-Amino-3-(thiophen-2-ylthio)propanoic acid;S-thiophenyl-l-cysteine;S-Thiophen-2-yl-L-cysteine;SCHEMBL503186;DTXSID50585039

Chemical Property of S-(2-Thienyl)-L-cysteine

Chemical Property:

• Vapor Pressure: 2.53E-06mmHg at 25°C
• PSA: 116.86000
• LogP: 1.95240
• Storage Temp.: 2-8°C
• XLogP3: -1.1
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 4
• Exact Mass: 203.00747088
• Heavy Atom Count: 12
• Complexity: 166

Purity/Quality:

98.5% ^*data from raw suppliers

S-(2-THIENYL)-L-CYSTEINE 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CSC(=C1)SCC(C(=O)O)N
• Isomeric SMILES: C1=CSC(=C1)SC[C@@H](C(=O)O)N

Technology Process of S-(2-Thienyl)-L-cysteine

There total 1 articles about S-(2-Thienyl)-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:

Reference yield:

Thiophene-2-thiol (7774-74-5) + L-phosphoserine (407-41-0,7331-08-0) → S-thienyl-L-cysteine (405150-23-4)

Guidance literature:

With ethylenediaminetetraacetic acid; O-phospho-L-serine sulfhydrylase from Aeropyrum pernix K₁; In aq. phosphate buffer; N,N-dimethyl-formamide; at 80 ℃; for 0.0166667h; pH=7.5; Enzymatic reaction;

DOI:10.1246/cl.170822

upstream raw materials:

Thiophene-2-thiol

L-phosphoserine