N-(2-benzoyl-4-chlorophenyl)-4-methylbenzenesulfonamide

Base Information

Chemical Name:N-(2-benzoyl-4-chlorophenyl)-4-methylbenzenesulfonamide
CAS No.:4873-59-0
Molecular Formula:C20H16ClNO3S
Molecular Weight:385.871
Hs Code.:
DSSTox Substance ID:DTXSID90359953
Nikkaji Number:J2.072.748I
Wikidata:Q82141406
ChEMBL ID:CHEMBL1603150
Mol file:4873-59-0.mol

Synonyms:4873-59-0;N-(2-benzoyl-4-chlorophenyl)-4-methylbenzenesulfonamide;Oprea1_269174;MLS000395018;CHEMBL1603150;SCHEMBL11182634;DTXSID90359953;Benzenesulfonamide, N-(2-benzoyl-4-chlorophenyl)-4-methyl-;HMS2552A22;AKOS001029260;SMR000248447;AB00546635-02;AG-670/31976033;Z54078781

Suppliers and Price of N-(2-benzoyl-4-chlorophenyl)-4-methylbenzenesulfonamide

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 2 raw suppliers

Chemical Property of N-(2-benzoyl-4-chlorophenyl)-4-methylbenzenesulfonamide

Chemical Property:

XLogP3:5.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:5
Exact Mass:385.0539422
Heavy Atom Count:26
Complexity:574

Purity/Quality:: 95% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC=C(C=C1)S(=O)(=O)NC2=C(C=C(C=C2)Cl)C(=O)C3=CC=CC=C3

Technology Process of N-(2-benzoyl-4-chlorophenyl)-4-methylbenzenesulfonamide

There total 11 articles about N-(2-benzoyl-4-chlorophenyl)-4-methylbenzenesulfonamide 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: 95.0%

: 719-59-5
5-chloro-2-aminobenzophenone

: 98-59-9
p-toluenesulfonyl chloride

: 4873-59-0
2-tosylamido-5-chlorobenzophenone

Guidance literature:: With hydrogenchloride; In pyridine; ethyl acetate; Petroleum ether;

Reference yield: 63.0%

: 824-79-3
sodium 4-methylbenzenesulfinate

: 719-64-2
5-chloro-3-phenylanthranil

: 4873-59-0
2-tosylamido-5-chlorobenzophenone

Guidance literature:: With water; iron(II) chloride; at 80 ℃; for 8h; Sealed tube;
DOI:10.1002/ejoc.202100010

Reference yield:

: 719-64-2
5-chloro-3-phenylanthranil

: 4873-59-0
2-tosylamido-5-chlorobenzophenone

Guidance literature:: Multi-step reaction with 2 steps

1: 75 percent / Fe; AcOH / H₂O; ethyl acetate / Heating

2: 69 percent / pyridine / 0.5 h / Heating

With pyridine; iron; acetic acid; In water; ethyl acetate;
DOI:10.1016/j.tet.2006.10.056