S-(N-Benzylthiocarbamoyl)cysteine

Base Information

Chemical Name:S-(N-Benzylthiocarbamoyl)cysteine
CAS No.:35446-36-7
Molecular Formula:C11H14 N2 O2 S2
Molecular Weight:270.376
Hs Code.:2930909090
DSSTox Substance ID:DTXSID90188947
Mol file:35446-36-7.mol

Synonyms:benzylisothiocyanate cysteine conjugate;S-(N-benzylthiocarbamoyl)-L-cysteine;S-(N-benzylthiocarbamoyl)cysteine

Suppliers and Price of S-(N-Benzylthiocarbamoyl)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-[N-Benzyl(thiocarbamoyl)]-L-cysteine
25 mg
$ 75.00

TRC
S-[N-Benzyl(thiocarbamoyl)]-L-cysteine
50 mg
$ 100.00

Medical Isotopes, Inc.
S-[N-Benzyl(thiocarbamoyl)]-L-cysteine
100 mg
$ 800.00

Biosynth Carbosynth
S-[N-Benzyl(thiocarbamoyl)]-L-cysteine
10 mg
$ 100.00

Biosynth Carbosynth
S-[N-Benzyl(thiocarbamoyl)]-L-cysteine
5 mg
$ 75.00

Biosynth Carbosynth
S-[N-Benzyl(thiocarbamoyl)]-L-cysteine
2 mg
$ 40.00

Biosynth Carbosynth
S-[N-Benzyl(thiocarbamoyl)]-L-cysteine
50 mg
$ 195.00

Biosynth Carbosynth
S-[N-Benzyl(thiocarbamoyl)]-L-cysteine
25 mg
$ 150.00

American Custom Chemicals Corporation
S-[N-BENZYL(THIOCARBAMOYL)]-L-CYSTEINE 95.00%
100MG
$ 290.85

AK Scientific
S-(N-Benzylthiocarbamoyl)cysteine
2mg
$ 104.00

Total 6 raw suppliers

Chemical Property of S-(N-Benzylthiocarbamoyl)cysteine

Chemical Property:

Vapor Pressure:3E-09mmHg at 25°C
Melting Point:191-193
Boiling Point:459.8 °C at 760 mmHg
Flash Point:231.9 °C
PSA：132.74000
Density:1.363 g/cm³
LogP:2.29740
Storage Temp.:−20°C
Solubility.:DMSO (Slightly, Sonicated)
XLogP3:-1
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:6
Exact Mass:270.04967004
Heavy Atom Count:17
Complexity:268

Purity/Quality:

98% ^*data from raw suppliers

S-[N-Benzyl(thiocarbamoyl)]-L-cysteine ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:Xi

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

Canonical SMILES:C1=CC=C(C=C1)CNC(=S)SCC(C(=O)O)N
Isomeric SMILES:C1=CC=C(C=C1)CNC(=S)SC[C@@H](C(=O)O)N
Uses Induction of Glutathione S-transerase (GST) activity by anticarcinogenic compounds is believed to be a major mechanism for carcinogen detoxification. S-[N-BENZYL(THIOCARBAMOYL)]-L-CYSTEINE has shown to induce Glutathione S- transerase activity in target organs of mice with no apparent toxic effects.

Technology Process of S-(N-Benzylthiocarbamoyl)cysteine

There total 3 articles about S-(N-Benzylthiocarbamoyl)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: 93.0%