5-Chloro-2-methoxy-4-nitrobenzene-1-sulfonyl chloride

Base Information

Chemical Name:5-Chloro-2-methoxy-4-nitrobenzene-1-sulfonyl chloride
CAS No.:62833-51-6
Molecular Formula:C7H5Cl2NO5S
Molecular Weight:286.092
Hs Code.:
DSSTox Substance ID:DTXSID90513013
Wikidata:Q82372521

Synonyms:62833-51-6;5-Chloro-2-methoxy-4-nitrobenzene-1-sulfonyl chloride;SCHEMBL11436791;DTXSID90513013;EN300-3337169

Suppliers and Price of 5-Chloro-2-methoxy-4-nitrobenzene-1-sulfonyl chloride

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 5-Chloro-2-methoxy-4-nitrobenzene-1-sulfonyl chloride

Chemical Property:

XLogP3:2.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:2
Exact Mass:284.9265488
Heavy Atom Count:16
Complexity:362

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=C(C=C(C(=C1)[N+](=O)[O-])Cl)S(=O)(=O)Cl

Technology Process of 5-Chloro-2-methoxy-4-nitrobenzene-1-sulfonyl chloride

There total 1 articles about 5-Chloro-2-methoxy-4-nitrobenzene-1-sulfonyl chloride 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:

: 62833-51-6
5-Chlor-2-methoxy-4-nitro-benzolsulfonylchlorid

Guidance literature:: 2-Amino-4-Chlor-5-nitro-anisol, 1. HNO2, 2. SO2, HCl;

Reference yield: 74.0%

: 62833-51-6
5-Chlor-2-methoxy-4-nitro-benzolsulfonylchlorid

: 6325-22-0,42286-14-6
chlorhydrate de (β-aminoethyl)-4 benzenesulfonamide

: 81514-25-2
5-Chloro-2-methoxy-4-nitro-N-[2-(4-sulfamoyl-phenyl)-ethyl]-benzenesulfonamide

Guidance literature:: With triethylamine; In diethyl ether; ethanol; for 0.75h; Heating;

Reference yield:

: 62833-51-6
5-Chlor-2-methoxy-4-nitro-benzolsulfonylchlorid

: 81514-37-6
C₁₉H₂₅ClN₄O₆S₂

Guidance literature:: Multi-step reaction with 3 steps

1: 74 percent / triethylamine / diethyl ether; ethanol / 0.75 h / Heating

2: 91 percent / Na₂CO₃ / acetone / 8 h / Heating

3: 95 percent / hydrogen / Pd-C / ethanol / Ambient temperature

With hydrogen; sodium carbonate; triethylamine; palladium on activated charcoal; In diethyl ether; ethanol; acetone;