3-Mercaptopropionyl-L-cysteine

Base Information

Chemical Name:3-Mercaptopropionyl-L-cysteine
CAS No.:65002-21-3
Molecular Formula:C₆H₁₁NO₃S₂
Molecular Weight:209.29
Hs Code.:
ChEMBL ID:CHEMBL309333
DSSTox Substance ID:DTXSID101306662

Synonyms:CHEMBL309333;3-Mercaptopropionyl-L-cysteine;SCHEMBL929193;OFHKDLLHCJDJSR-BYPYZUCNSA-N;DTXSID101306662;N-(3-Mercaptopropanoyl)-L-cysteine;BDBM50406946;65002-21-3

Suppliers and Price of 3-Mercaptopropionyl-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
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price

Total 0 raw suppliers

Chemical Property of 3-Mercaptopropionyl-L-cysteine

Chemical Property:

XLogP3:-0.3
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:5
Exact Mass:209.01803556
Heavy Atom Count:12
Complexity:174

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C(CS)C(=O)NC(CS)C(=O)O
Isomeric SMILES:C(CS)C(=O)N[C@@H](CS)C(=O)O

Technology Process of 3-Mercaptopropionyl-L-cysteine

There total 1 articles about 3-Mercaptopropionyl-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:

: 52-90-4
L-Cysteine

: 107-96-0
3-mercaptopropionic acid

: 65002-21-3
N-(3-mercaptopropionyl)-L-cysteine

: 78818-54-9
(5R)-3-cyclohexyl-2-cyclohexylimino-5-mercaptomethyl-4-imidazolidinone hydrochloride

Guidance literature:: With potassium carbonate; dicyclohexyl-carbodiimide; Yield given. Multistep reaction; 1.) EtOAc, r.t., 1 h; 1.) EtOAc, MeOH, water, r.t., 4 h;
DOI:10.1248/cpb.29.940