4-Chloro-N-hydroxybenzene-1-carbothioamide

Base Information

Chemical Name:4-Chloro-N-hydroxybenzene-1-carbothioamide
CAS No.:13749-89-8
Molecular Formula:C₇H₆ClNOS
Molecular Weight:187.65
Hs Code.:
DSSTox Substance ID:DTXSID20505229
Wikidata:Q82360194

Synonyms:13749-89-8;4-Chloro-N-hydroxybenzene-1-carbothioamide;DTXSID20505229

Suppliers and Price of 4-Chloro-N-hydroxybenzene-1-carbothioamide

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 1 raw suppliers

Chemical Property of 4-Chloro-N-hydroxybenzene-1-carbothioamide

Chemical Property:

XLogP3:1.9
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:186.9858627
Heavy Atom Count:11
Complexity:145

Purity/Quality:: 99.90% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC(=CC=C1C(=S)NO)Cl

Technology Process of 4-Chloro-N-hydroxybenzene-1-carbothioamide

There total 4 articles about 4-Chloro-N-hydroxybenzene-1-carbothioamide 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:

: 13915-60-1
O-ethyl 4-chlorobenzenecarbothioate

: 13749-89-8
4-Chlor-benzothiohydroxamsaeure

Guidance literature:: With hydroxylamine hydrochloride; sodium methylate;

Reference yield:

: 13749-89-8
4-chloro-N-hydroxy-thiobenzamide

Guidance literature:: With hydroxylamine;

Reference yield:

: 40546-41-6
ethyl-4-chlorobenzimidate hydrochloride

: 13749-89-8
4-Chlor-benzothiohydroxamsaeure

Guidance literature:: Multi-step reaction with 2 steps

1: H₂S, Py

2: NH₂OH*HCl, NaOMe

With pyridine; hydrogen sulfide; hydroxylamine hydrochloride; sodium methylate;