Carbamic acid, (2-mercaptoethyl)-, phenylmethyl ester

Base Information

Chemical Name:Carbamic acid, (2-mercaptoethyl)-, phenylmethyl ester
CAS No.:68642-94-4
Molecular Formula:C10H13NO2S
Molecular Weight:211.285
Hs Code.:
DSSTox Substance ID:DTXSID40510153
Wikidata:Q82368259

Synonyms:68642-94-4;Carbamic acid, (2-mercaptoethyl)-, phenylmethyl ester;BENZYL N-(2-SULFANYLETHYL)CARBAMATE;benzyl (2-mercaptoethyl)carbamate;SCHEMBL6546647;DTXSID40510153;Benzyl (2-sulfanylethyl)carbamate;AKOS028112196;EN300-8782360

Suppliers and Price of Carbamic acid, (2-mercaptoethyl)-, phenylmethyl ester

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 Carbamic acid, (2-mercaptoethyl)-, phenylmethyl ester

Chemical Property:

XLogP3:2
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:5
Exact Mass:211.06669983
Heavy Atom Count:14
Complexity:170

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)COC(=O)NCCS

Technology Process of Carbamic acid, (2-mercaptoethyl)-, phenylmethyl ester

There total 2 articles about Carbamic acid, (2-mercaptoethyl)-, phenylmethyl ester 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:

: 501-53-1,94274-21-2
benzyl chloroformate

: 60-23-1
Cysteamine

: 68642-94-4
2-(benzyloxycarbonylamino)-1-ethanethiol

Guidance literature:: With sodium hydroxide; In toluene;
DOI:10.1021/jm00187a022

Reference yield:

: 156-57-0
2-mercaptoethylamine hydrochloride

: 68642-94-4
2-(benzyloxycarbonylamino)-1-ethanethiol

Guidance literature:: Yield given. Multistep reaction;
DOI:10.1055/s-1980-29273

Reference yield: 94.0%

: 68642-94-4
2-(benzyloxycarbonylamino)-1-ethanethiol

: benzyl (ethyl-2-d)carbamate

Guidance literature:: With di-tert-butyl peroxide; water-d2; ethydiphenylphosphine oxide; In chloroform; at 20 ℃; for 6h; Sealed tube; Irradiation;