N-Hydroxybenzenecarbothioamide

Base Information

Chemical Name:N-Hydroxybenzenecarbothioamide
CAS No.:15177-34-1
Molecular Formula:C7H7NOS
Molecular Weight:153.205
Hs Code.:
DSSTox Substance ID:DTXSID60505228
Nikkaji Number:J3.332.301H
Mol file:15177-34-1.mol

Synonyms:N-Hydroxybenzenecarbothioamide;Thiobenzoylhydroxylamin;15177-34-1;benzothiohydroxamic acid;SCHEMBL3079333;SCHEMBL11809875;DTXSID60505228;FBYRYEFDOMKFEE-UHFFFAOYSA-N

Suppliers and Price of N-Hydroxybenzenecarbothioamide

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 N-Hydroxybenzenecarbothioamide

Chemical Property:

XLogP3:0.9
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:153.02483502
Heavy Atom Count:10
Complexity:121

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C(=S)NO

Technology Process of N-Hydroxybenzenecarbothioamide

There total 11 articles about N-Hydroxybenzenecarbothioamide 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: 87.0%

: 698-16-8
benzohydroximoyl chloride

: 15177-34-1
thiobenzhydroxamic acid

Guidance literature:: With sodium sulfide; triethylamine; In diethyl ether; water; at 20 ℃; for 1h;
DOI:10.1021/jo500080x

Reference yield: 66.0%

: 75-15-0,12122-00-8
carbon disulfide

: 108-86-1,52753-63-6
bromobenzene

: 15177-34-1
thiobenzhydroxamic acid

Guidance literature:: bromobenzene; With iodine; magnesium; In diethyl ether; for 0.5h; Reflux;

carbon disulfide; In diethyl ether; at 0 ℃; Reflux;

With hydroxylamine hydrochloride; In water;
DOI:10.1002/jms.1711