N-Benzyl-3-chloro-benzenesulfonamide

Base Information

Chemical Name:N-Benzyl-3-chloro-benzenesulfonamide
CAS No.:16937-20-5
Molecular Formula:C₁₃H₁₂ClNO₂S
Molecular Weight:281.763
Hs Code.:
DSSTox Substance ID:DTXSID001263893

Synonyms:N-Benzyl-3-chloro-benzenesulfonamide;16937-20-5;N-benzyl-3-chlorobenzene-1-sulfonamide;N-benzyl-3-chlorobenzenesulfonamide;DTXSID001263893;HMS1725B05;STL191156;AKOS016598013;3-Chloro-N-(phenylmethyl)benzenesulfonamide;EN300-07445;Z45508808

Suppliers and Price of N-Benzyl-3-chloro-benzenesulfonamide

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 N-Benzyl-3-chloro-benzenesulfonamide

Chemical Property:

XLogP3:3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:281.0277275
Heavy Atom Count:18
Complexity:347

Purity/Quality:

Safty Information:

Pictogram(s):
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MSDS Files:

Useful:

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

Technology Process of N-Benzyl-3-chloro-benzenesulfonamide

There total 1 articles about N-Benzyl-3-chloro-benzenesulfonamide 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: 85.0%

: 17260-71-8
3-chloro-benzenesulfonamide

: 100-51-6,185532-71-2
benzyl alcohol

: 16937-20-5
N-benzyl-3-chlorobenzenesulfonamide

Guidance literature:: With [(η⁵-C₅Me₅)Ir(6,6'-dihydroxy-2,2'-bipyridine)(H₂O)]OTf₂; caesium carbonate; In water; at 120 ℃; for 15h; Inert atmosphere; Schlenk technique;
DOI:10.1002/adsc.201300711