Benzenesulfonamide, 4-methyl-N-[[4-(trifluoromethyl)phenyl]methylene]-

Base Information

Chemical Name:Benzenesulfonamide, 4-methyl-N-[[4-(trifluoromethyl)phenyl]methylene]-
CAS No.:198012-02-1
Molecular Formula:C15H12F3NO2S
Molecular Weight:327.327
Hs Code.:
DSSTox Substance ID:DTXSID60352153
Nikkaji Number:J899.156A

Synonyms:Benzenesulfonamide, 4-methyl-N-[[4-(trifluoromethyl)phenyl]methylene]-;198012-02-1;CBMicro_046102;DTXSID60352153;PORBHQWXDLUOLN-UHFFFAOYSA-N

Suppliers and Price of Benzenesulfonamide, 4-methyl-N-[[4-(trifluoromethyl)phenyl]methylene]-

Supply Marketing:

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

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Chemical Property of Benzenesulfonamide, 4-methyl-N-[[4-(trifluoromethyl)phenyl]methylene]-

Chemical Property:

XLogP3:4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:3
Exact Mass:327.05408429
Heavy Atom Count:22
Complexity:480

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC=C(C=C1)S(=O)(=O)N=CC2=CC=C(C=C2)C(F)(F)F

Technology Process of Benzenesulfonamide, 4-methyl-N-[[4-(trifluoromethyl)phenyl]methylene]-

There total 7 articles about Benzenesulfonamide, 4-methyl-N-[[4-(trifluoromethyl)phenyl]methylene]- 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: 100.0%

: 4-methyl-N-[(toluene-4-sulfonyl)-(4-trifluoromethyl-phenyl)-methyl]-benzenesulfonamide

: 198012-02-1
(E)-4-methyl-N-(4-(trifluoromethyl)benzylidene)benzenesulfonamide

Guidance literature:: With sodium hydrogencarbonate; In dichloromethane; at 20 ℃; for 2h;
DOI:10.1080/00397910601131387

Reference yield: 99.0%

: 455-19-6
4-Trifluoromethylbenzaldehyde

: 55962-05-5
[N-(p-tolylsulfonyl)imino]phenyliodinane

: 198012-02-1
4-methyl-N-(4-trifluoromethylbenzylidene)-benzenesulfonamide

Guidance literature:: With pyridine; copper(l) chloride; In dichloromethane; at 20 ℃; for 18h; Molecular sieve; Inert atmosphere;
DOI:10.1021/jo200284a

Reference yield: 90.0%

: 455-19-6
4-Trifluoromethylbenzaldehyde

: 70-55-3
toluene-4-sulfonamide

: 198012-02-1
4-methyl-N-(4-trifluoromethylbenzylidene)-benzenesulfonamide

Guidance literature:: With silica-supported iron oxide; In toluene; at 100 ℃; for 1h; Schlenk technique; Inert atmosphere;
DOI:10.1016/j.crci.2019.06.005