S-(2-Thiazolyl)-L-cysteine

Base Information

Chemical Name:S-(2-Thiazolyl)-L-cysteine
CAS No.:405150-20-1
Molecular Formula:C6H8N2O2S2
Molecular Weight:204.27000
Hs Code.:2934100090
DSSTox Substance ID:DTXSID10431462
Mol file:405150-20-1.mol

Synonyms:S-(2-Thiazolyl)-L-cysteine;405150-20-1;(2R)-2-AMINO-3-(1,3-THIAZOL-2-YLSULFANYL)PROPANOIC ACID;(R)-2-Amino-3-(thiazol-2-ylthio)propanoic acid;(R)-2-Amino-3-(2-thiazolylthio)propionic acid;SCHEMBL503349;DTXSID10431462;STR07174;S-(2-Thiazolyl)-L-cysteine, produced by Wacker Chemie AG, Burghausen, Germany, >=95.0% (HPLC)

Suppliers and Price of S-(2-Thiazolyl)-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

TRC
S-2-Thiazolyl-L-cysteine
500mg
$ 1470.00

Sigma-Aldrich
S-(2-Thiazolyl)-L-cysteine produced by Wacker Chemie AG, Burghausen, Germany, ≥95.0% (HPLC)
1g-f
$ 153.00

American Custom Chemicals Corporation
S-(2-THIAZOLYL)-L-CYSTEINE 95.00%
1G
$ 790.71

Total 11 raw suppliers

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

Chemical Property:

Vapor Pressure:0mmHg at 25°C
PSA：129.75000
LogP:1.34740
Storage Temp.:2-8°C
XLogP3:-1.8
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:4
Exact Mass:204.00271985
Heavy Atom Count:12
Complexity:168

Purity/Quality:

99% ^*data from raw suppliers

S-2-Thiazolyl-L-cysteine ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CSC(=N1)SCC(C(=O)O)N
Isomeric SMILES:C1=CSC(=N1)SC[C@@H](C(=O)O)N
Uses S-2-Thiazolyl-L-cysteine is used in the semisynthetic production of unnatural L-α-amino acids by metabolic engineering of the cysteine-biosynthetic pathway.

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

There total 2 articles about S-(2-Thiazolyl)-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:

: 407-41-0,7331-08-0
L-phosphoserine

: 5685-05-2
2-mercaptothiazole

: 405150-20-1
S-(2-thiazolyl)-L-cysteine

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 0.05h; pH=7.5; Enzymatic reaction;
DOI:10.1246/cl.170822

Reference yield:

: 5147-00-2,25248-96-8,44901-25-9
O-acetyl-L-serine

: 5685-05-2
2-mercaptothiazole

: 405150-20-1
S-(2-thiazolyl)-L-cysteine

Guidance literature:: With pyridoxal 5'-phosphate; cysteine synthase from Escherichia coli; In aq. phosphate buffer; at 37 ℃; pH=6.4 - 7; Enzymatic reaction;
DOI:10.1002/anie.202014540