Benzamide, 2,5-dichloro-N-[4-[(dimethylamino)sulfonyl]phenyl]-

Base Information

Chemical Name:Benzamide, 2,5-dichloro-N-[4-[(dimethylamino)sulfonyl]phenyl]-
CAS No.:89564-68-1
Molecular Formula:C₁₅H₁₄Cl₂N₂O₃S
Molecular Weight:373.26
Hs Code.:
DSSTox Substance ID:DTXSID80429452
Wikidata:Q82242490

Synonyms:89564-68-1;Benzamide, 2,5-dichloro-N-[4-[(dimethylamino)sulfonyl]phenyl]-;DTXSID80429452;AKOS017068068

Suppliers and Price of Benzamide, 2,5-dichloro-N-[4-[(dimethylamino)sulfonyl]phenyl]-

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of Benzamide, 2,5-dichloro-N-[4-[(dimethylamino)sulfonyl]phenyl]-

Chemical Property:

XLogP3:3.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:4
Exact Mass:372.0102189
Heavy Atom Count:23
Complexity:513

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CN(C)S(=O)(=O)C1=CC=C(C=C1)NC(=O)C2=C(C=CC(=C2)Cl)Cl

Technology Process of Benzamide, 2,5-dichloro-N-[4-[(dimethylamino)sulfonyl]phenyl]-

There total 2 articles about Benzamide, 2,5-dichloro-N-[4-[(dimethylamino)sulfonyl]phenyl]- 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: 64.0%

: 89564-65-8
N⁴-(2,5-Dichlorobenzoyl)sulfanilyl chloride

: 124-40-3
dimethyl amine

: 89564-68-1
2,5-Dichloro-N-(4-dimethylsulfamoyl-phenyl)-benzamide

Guidance literature:

Reference yield:

: 6043-41-0
2,5-Dichlorobenzanilide

: 89564-68-1
2,5-Dichloro-N-(4-dimethylsulfamoyl-phenyl)-benzamide

Guidance literature:: Multi-step reaction with 2 steps

1: 65 percent / chlorosulfonic acid / 3 h / 40 - 60 °C

2: 64 percent

With chlorosulfonic acid;