N-(4-Nitrophenyl)benzenecarbothioamide

Base Information

Chemical Name:N-(4-Nitrophenyl)benzenecarbothioamide
CAS No.:5265-19-0
Molecular Formula:C13H10N2O2S
Molecular Weight:258.301
Hs Code.:
DSSTox Substance ID:DTXSID80523005
Wikidata:Q82388761
Mol file:5265-19-0.mol

Synonyms:N-(4-Nitrophenyl)benzenecarbothioamide;p-nitrothiobenzanilide;5265-19-0;SCHEMBL5047835;DTXSID80523005

Suppliers and Price of N-(4-Nitrophenyl)benzenecarbothioamide

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 2 raw suppliers

Chemical Property of N-(4-Nitrophenyl)benzenecarbothioamide

Chemical Property:

XLogP3:2.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:258.04629874
Heavy Atom Count:18
Complexity:303

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C(=S)NC2=CC=C(C=C2)[N+](=O)[O-]

Technology Process of N-(4-Nitrophenyl)benzenecarbothioamide

There total 10 articles about N-(4-Nitrophenyl)benzenecarbothioamide 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: 62.0%

: 3393-96-2
p-nitrobenzanilide

: 5265-19-0
N-(4-nitrophenyl)thiobenzamide

Guidance literature:: With Lawessons reagent; In toluene; for 29h; Inert atmosphere; Reflux;
DOI:10.1021/ol802033p

Reference yield: 40.0%

: 100-52-7
benzaldehyde

: 100-01-6,104810-17-5
4-nitro-aniline

: 5265-19-0
N-(4-nitrophenyl)thiobenzamide

Guidance literature:: With sodium sulfide; sulfur; In N,N-dimethyl-formamide; at 115 ℃; for 12h;
DOI:10.1055/s-2007-991073

Reference yield: 35.0%

: 40611-33-4
N-benzoyl-N'-(4-nitrophenyl)thiourea

: 5265-19-0
N-(4-nitrophenyl)thiobenzamide

: 3393-96-2
p-nitrobenzanilide

Guidance literature:: With iodine-alumina; In neat (no solvent); at 100 ℃; for 0.25h; Overall yield = 84 %; Microwave irradiation;
DOI:10.1039/c4nj02021a