4-[(4-Nitrophenyl)disulfanyl]aniline

Base Information

Chemical Name:4-[(4-Nitrophenyl)disulfanyl]aniline
CAS No.:40897-48-1
Molecular Formula:C12H10N2O2S2
Molecular Weight:278.356
Hs Code.:
DSSTox Substance ID:DTXSID10532009
Nikkaji Number:J1.049.825B
Wikidata:Q82404290
Mol file:40897-48-1.mol

Synonyms:4-[(4-Nitrophenyl)disulfanyl]aniline;40897-48-1;4-amino-4'-nitrodiphenyl disulfide;SCHEMBL11856128;DTXSID10532009

Suppliers and Price of 4-[(4-Nitrophenyl)disulfanyl]aniline

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 0 raw suppliers

Chemical Property of 4-[(4-Nitrophenyl)disulfanyl]aniline

Chemical Property:

XLogP3:3.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:3
Exact Mass:278.01836991
Heavy Atom Count:18
Complexity:270

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC(=CC=C1N)SSC2=CC=C(C=C2)[N+](=O)[O-]

Technology Process of 4-[(4-Nitrophenyl)disulfanyl]aniline

There total 5 articles about 4-[(4-Nitrophenyl)disulfanyl]aniline 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: 84.0%

: 1849-36-1
para-nitrobenzenethiol

: 1193-02-8
4-aminotiophenol

: 40897-48-1
4-aminophenyl 4'-nitrophenyl disulfide

Guidance literature:: With manganese(II)carbonate; 3,4,5-trihydroxybenzoic acid; oxygen; sodium carbonate; In water; at 80 ℃; for 4h; under 2250.23 Torr; pH=9; Schlenk technique; Green chemistry;
DOI:10.1039/c9gc00091g