2-[(2-Chloro-4-nitrophenyl)sulfanyl]-N,4-dimethylaniline

Base Information

Chemical Name:2-[(2-Chloro-4-nitrophenyl)sulfanyl]-N,4-dimethylaniline
CAS No.:79226-42-9
Molecular Formula:C14H13ClN2O2S
Molecular Weight:308.788
Hs Code.:
DSSTox Substance ID:DTXSID80508175
Wikidata:Q82364902

Synonyms:79226-42-9;2-[(2-Chloro-4-nitrophenyl)sulfanyl]-N,4-dimethylaniline;DTXSID80508175

Suppliers and Price of 2-[(2-Chloro-4-nitrophenyl)sulfanyl]-N,4-dimethylaniline

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 2-[(2-Chloro-4-nitrophenyl)sulfanyl]-N,4-dimethylaniline

Chemical Property:

XLogP3:4.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:3
Exact Mass:308.0386265
Heavy Atom Count:20
Complexity:340

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC(=C(C=C1)NC)SC2=C(C=C(C=C2)[N+](=O)[O-])Cl

Technology Process of 2-[(2-Chloro-4-nitrophenyl)sulfanyl]-N,4-dimethylaniline

There total 4 articles about 2-[(2-Chloro-4-nitrophenyl)sulfanyl]-N,4-dimethylaniline 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: 75.0%

: 99-54-7
3,4-dichloronitrobenzene

: 79226-39-4
5-Methyl-2-methylamino-benzenethiol

: 79226-42-9
[2-(2-Chloro-4-nitro-phenylsulfanyl)-4-methyl-phenyl]-methyl-amine

Guidance literature:: With sodium carbonate; In ethanol; for 10h; Heating;
DOI:10.1002/jhet.5570180425

Reference yield:

: 2536-91-6
6-methylbenzothiazol-2-ylamine

: 79226-42-9
[2-(2-Chloro-4-nitro-phenylsulfanyl)-4-methyl-phenyl]-methyl-amine

Guidance literature:: Multi-step reaction with 3 steps

1: 76 percent / ethanol / 15 h / Heating

2: 50percent aq. KOH / Heating

3: 75 percent / sodium carbonate / ethanol / 10 h / Heating

With potassium hydroxide; sodium carbonate; In ethanol;
DOI:10.1002/jhet.5570180425

Reference yield:

: 79226-35-0
3,6-Dimethyl-3H-benzothiazol-2-ylideneamine; hydriodide

: 79226-42-9
[2-(2-Chloro-4-nitro-phenylsulfanyl)-4-methyl-phenyl]-methyl-amine

Guidance literature:: Multi-step reaction with 2 steps

1: 50percent aq. KOH / Heating

2: 75 percent / sodium carbonate / ethanol / 10 h / Heating

With potassium hydroxide; sodium carbonate; In ethanol;
DOI:10.1002/jhet.5570180425