Cysteine-S-Acetamide

Base Information

Chemical Name:Cysteine-S-Acetamide
CAS No.:17528-66-4
Molecular Formula:C₅H₁₀N₂O₃S
Molecular Weight:178.212
Hs Code.:
UNII:LAH55Q7GIH
Metabolomics Workbench ID:147533
Nikkaji Number:J1.303.808B
Wikidata:Q27093959
Mol file:17528-66-4.mol

Synonyms:S-carbamidomethylcysteine

Suppliers and Price of Cysteine-S-Acetamide

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 6 raw suppliers

Chemical Property of Cysteine-S-Acetamide

Chemical Property:

Vapor Pressure:4.01E-09mmHg at 25°C
Boiling Point:444°Cat760mmHg
Flash Point:222.3°C
PSA：131.71000
Density:1.431g/cm³
LogP:0.01740
XLogP3:-3.8
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:5
Exact Mass:178.04121336
Heavy Atom Count:11
Complexity:162

Purity/Quality:: 95% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

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

Technology Process of Cysteine-S-Acetamide

There total 2 articles about Cysteine-S-Acetamide 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

: 144-48-9
iodacetamide

: 17528-66-4
cysteine

Guidance literature:

Reference yield:

: 52-90-4
L-Cysteine

: 79-07-2
Chloroacetamide

: 17528-66-4
cysteine

Guidance literature:: DOI:10.1021/jo01103a004

Reference yield:

: 17528-66-4
cysteine

: 41117-61-7
p-Nitrophenyl N^α-Boc-S-carbamidomethylcystein

Guidance literature:: Multi-step reaction with 2 steps

1: aq. NaOH / dioxane

2: DCC / dimethylformamide

With sodium hydroxide; dicyclohexyl-carbodiimide; In 1,4-dioxane; N,N-dimethyl-formamide;
DOI:10.1021/jo00960a026