4-Thiazolidinecarboxylic acid, 3-(2-mercapto-1-oxopropyl)-, (S-(R,S))-

Base Information

Chemical Name:4-Thiazolidinecarboxylic acid, 3-(2-mercapto-1-oxopropyl)-, (S-(R*,S*))-
CAS No.:67714-44-7
Molecular Formula:C7H11NO3S2
Molecular Weight:221.2971
Hs Code.:
DSSTox Substance ID:DTXSID20217991
Nikkaji Number:J395.199E
Wikidata:Q83094716
ChEMBL ID:CHEMBL486546
Mol file:67714-44-7.mol

Synonyms:67714-44-7;4-Thiazolidinecarboxylic acid, 3-(2-mercapto-1-oxopropyl)-, (S-(R*,S*))-;SA 300;CHEMBL486546;SCHEMBL11003689;DTXSID20217991;LXQJJKNBGQICEQ-WHFBIAKZSA-N;(4r)-3-[(2s)-2-mercapto-propanoyl]-4-thiazolidinecarboxylic acid;(4R)-3-[(2S)-2-mercaptopropanoyl]-4-thiazolidinecarboxylic acid

Suppliers and Price of 4-Thiazolidinecarboxylic acid, 3-(2-mercapto-1-oxopropyl)-, (S-(R*,S*))-

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 3 raw suppliers

Chemical Property of 4-Thiazolidinecarboxylic acid, 3-(2-mercapto-1-oxopropyl)-, (S-(R*,S*))-

Chemical Property:

Vapor Pressure:3.98E-10mmHg at 25°C
Melting Point:122-123 °C(Solv: ethyl acetate (141-78-6))
Boiling Point:469.8°Cat760mmHg
PKA:3.02±0.20(Predicted)
Flash Point:238°C
PSA：121.71000
Density:1.439g/cm³
LogP:0.22870
XLogP3:0.6
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:2
Exact Mass:221.01803556
Heavy Atom Count:13
Complexity:234

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C(=O)N1CSCC1C(=O)O)S
Isomeric SMILES:C[C@@H](C(=O)N1CSC[C@H]1C(=O)O)S

Technology Process of 4-Thiazolidinecarboxylic acid, 3-(2-mercapto-1-oxopropyl)-, (S-(R*,S*))-

There total 3 articles about 4-Thiazolidinecarboxylic acid, 3-(2-mercapto-1-oxopropyl)-, (S-(R*,S*))- 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: 92.0%