N-phenyl-2-benzoylbenzenesulfonamide imine

Base Information

Chemical Name:N-phenyl-2-benzoylbenzenesulfonamide imine
CAS No.:18963-20-7
Molecular Formula:C19H16N2O2S
Molecular Weight:336.4075
Hs Code.:
NSC Number:108403
Mol file:18963-20-7.mol

Synonyms:NSC108403;NSC-108403;18963-20-7;N-phenyl-2-benzoylbenzenesulfonamide imine

Suppliers and Price of N-phenyl-2-benzoylbenzenesulfonamide imine

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-phenyl-2-benzoylbenzenesulfonamide imine

Chemical Property:

Vapor Pressure:1.58E-10mmHg at 25°C
Boiling Point:510.2°C at 760 mmHg
Flash Point:262.4°C
Density:1.22g/cm³
XLogP3:3.9
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:5
Exact Mass:336.09324893
Heavy Atom Count:24
Complexity:514

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C(=N)C2=CC=CC=C2S(=O)(=O)NC3=CC=CC=C3

Technology Process of N-phenyl-2-benzoylbenzenesulfonamide imine

There total 3 articles about N-phenyl-2-benzoylbenzenesulfonamide imine 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: 53.0%

: 18963-22-9
2-Phenyl-3-amino-3-phenylbenzoisothiazoline 1,1-dioxide

: 18963-20-7
N-Phenyl-2-benzoylbenzenesulfonamide

Guidance literature:: at 140 ℃; for 0.166667h;
DOI:10.1007/BF00505593

Reference yield:

: 1678-25-7
N-phenylbenzenesulfonamide

: 18963-20-7
N-Phenyl-2-benzoylbenzenesulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: 24 percent / n-Butyllithium / tetrahydrofuran; diethyl ether / 1) 0 deg C, l,5 h, 2) 1 h.

2: 53 percent / 0.17 h / 140 °C

With n-butyllithium; In tetrahydrofuran; diethyl ether;
DOI:10.1007/BF00505593

Reference yield:

: 100-47-0
benzonitrile

: 18963-20-7
N-Phenyl-2-benzoylbenzenesulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: 24 percent / n-Butyllithium / tetrahydrofuran; diethyl ether / 1) 0 deg C, l,5 h, 2) 1 h.

2: 53 percent / 0.17 h / 140 °C

With n-butyllithium; In tetrahydrofuran; diethyl ether;
DOI:10.1007/BF00505593