N-[ethyl(phenyl)-lambda~4~-sulfanylidene]-4-methylbenzenesulfonamide

Base Information

Chemical Name:N-[ethyl(phenyl)-lambda~4~-sulfanylidene]-4-methylbenzenesulfonamide
CAS No.:10330-18-4
Molecular Formula:C15H17 N O2 S2
Molecular Weight:307.437
Hs Code.:
NSC Number:152584
Mol file:10330-18-4.mol

Synonyms:10330-18-4;N-[ethyl(phenyl)-lambda~4~-sulfanylidene]-4-methylbenzenesulfonamide;(NE)-N-[ethyl(phenyl)-lambda4-sulfanylidene]-4-methylbenzenesulfonamide;NSC152584;MLS000849840;HMS1661P12;HMS2791E12;CCG-242582;NSC-152584;SMR000455858

Suppliers and Price of N-[ethyl(phenyl)-lambda~4~-sulfanylidene]-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-[ethyl(phenyl)-lambda~4~-sulfanylidene]-4-methylbenzenesulfonamide

Chemical Property:

Vapor Pressure:5.77E-09mmHg at 25°C
Boiling Point:481.5°C at 760 mmHg
Flash Point:245°C
Density:1.21g/cm³
XLogP3:4.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:4
Exact Mass:307.07007113
Heavy Atom Count:20
Complexity:425

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCS(=NS(=O)(=O)C1=CC=C(C=C1)C)C2=CC=CC=C2
Isomeric SMILES:CC/S(=N\S(=O)(=O)C1=CC=C(C=C1)C)/C2=CC=CC=C2

Technology Process of N-[ethyl(phenyl)-lambda~4~-sulfanylidene]-4-methylbenzenesulfonamide

There total 8 articles about N-[ethyl(phenyl)-lambda~4~-sulfanylidene]-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%

: 622-38-8
Ethyl phenyl sulfide

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

: 10330-18-4,386737-39-9
S-ethyl-S-phenyl-N-(p-tolylsulfonyl)sulfimide

Guidance literature:: With iron(III) tris(4-chloro-2,6-dimethyl-3,5-heptanedionate); 2,6-bis[(4R)-5,5-dihydro-4-phenyl-2-oxazolyl]pyridine; In acetone; at -20 ℃; for 28h; enantioselective reaction;
DOI:10.1002/anie.201304451

Reference yield: 12.0%

: 941-55-9
4-toluenesulfonyl azide

: 622-38-8
Ethyl phenyl sulfide

: 10330-18-4
Aethyl-phenyl-N-p-toluolsulphonylsulphilimin

Guidance literature:: cis-β Ru(salalen)(CO)2 complex; In dichloromethane; at 20 ℃; for 24h; Irradiation;
DOI:10.1246/cl.2007.1092

Reference yield:

: 941-55-9
4-toluenesulfonyl azide

: 622-38-8
Ethyl phenyl sulfide

: 10330-18-4
S-Ethyl-S-phenyl-N-p-tolylsulfonyl-sulfilimin

Guidance literature:: With D-glucose; cytochrome P-I₂₆₃F V₈₇A A₃₂₈V variant; NADPH; In aq. phosphate buffer; dimethyl sulfoxide; at 20 ℃; for 20h; pH=8; Reagent/catalyst; Enzymatic reaction;
DOI:10.1002/anie.201601056