N-[4-(Benzylsulfamoyl)phenyl]-3,4-dichlorobenzamide

Base Information

Chemical Name:N-[4-(Benzylsulfamoyl)phenyl]-3,4-dichlorobenzamide
CAS No.:89565-02-6
Molecular Formula:C₂₀H₁₆Cl₂N₂O₃S
Molecular Weight:435.331
Hs Code.:
DSSTox Substance ID:DTXSID60536517
Wikidata:Q82411218

Synonyms:89565-02-6;N-[4-(Benzylsulfamoyl)phenyl]-3,4-dichlorobenzamide;DTXSID60536517

Suppliers and Price of N-[4-(Benzylsulfamoyl)phenyl]-3,4-dichlorobenzamide

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
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Total 0 raw suppliers

Chemical Property of N-[4-(Benzylsulfamoyl)phenyl]-3,4-dichlorobenzamide

Chemical Property:

XLogP3:4.9
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:6
Exact Mass:434.0258689
Heavy Atom Count:28
Complexity:611

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)CNS(=O)(=O)C2=CC=C(C=C2)NC(=O)C3=CC(=C(C=C3)Cl)Cl

Technology Process of N-[4-(Benzylsulfamoyl)phenyl]-3,4-dichlorobenzamide

There total 2 articles about N-[4-(Benzylsulfamoyl)phenyl]-3,4-dichlorobenzamide 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: 90.0%

: 89564-67-0
4-(3,4-Dichloro-benzoylamino)-benzenesulfonyl chloride

: 100-46-9
benzylamine

: 89565-02-6
N-(4-Benzylsulfamoyl-phenyl)-3,4-dichloro-benzamide

Guidance literature:

Reference yield:

: 6043-42-1
3,4-dichloro-N-phenylbenzamide

: 89565-02-6
N-(4-Benzylsulfamoyl-phenyl)-3,4-dichloro-benzamide

Guidance literature:: Multi-step reaction with 2 steps

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

2: 90 percent

With chlorosulfonic acid;