Sulfilimine, S-phenyl-S-propyl-N-(p-tolylsulfonyl)-

Base Information

Chemical Name:Sulfilimine, S-phenyl-S-propyl-N-(p-tolylsulfonyl)-
CAS No.:18922-55-9
Molecular Formula:C16H19NO2S2
Molecular Weight:321.4576
Hs Code.:
NSC Number:99140

Synonyms:Sulfilimine, S-phenyl-S-propyl-N-(p-tolylsulfonyl)-;18922-55-9;(NE)-4-methyl-N-[phenyl(propyl)-lambda4-sulfanylidene]benzenesulfonamide;Sulfilimine, N-[(4-methylphenyl)sulfonyl]-S-phenyl-S-propyl-;NSC99140;NSC-99140;CCG-242587

Suppliers and Price of Sulfilimine, S-phenyl-S-propyl-N-(p-tolylsulfonyl)-

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 6 raw suppliers

Chemical Property of Sulfilimine, S-phenyl-S-propyl-N-(p-tolylsulfonyl)-

Chemical Property:

Vapor Pressure:2.57E-09mmHg at 25°C
Boiling Point:491.2°C at 760 mmHg
Flash Point:250.9°C
Density:1.19g/cm³
XLogP3:5.3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:5
Exact Mass:321.08572120
Heavy Atom Count:21
Complexity:439

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

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

Technology Process of Sulfilimine, S-phenyl-S-propyl-N-(p-tolylsulfonyl)-

There total 4 articles about Sulfilimine, S-phenyl-S-propyl-N-(p-tolylsulfonyl)- 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: 89.0%

: 874-79-3
phenyl(propyl)sulfide

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

: 18922-55-9
S-(n-propyl)-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 16h; enantioselective reaction;
DOI:10.1002/anie.201304451

Reference yield:

: 941-55-9
4-toluenesulfonyl azide

: 874-79-3
phenyl(propyl)sulfide

: 18922-55-9
S-(n-propyl)-S-phenyl-N-(4-methylbenzenesulfonyl)sulfimide

Guidance literature:: With D-glucose; cytochrome P-I₂₆₃F V₈₇A A₃₂₈VA 268G A₈₂I variant; NADPH; In aq. phosphate buffer; dimethyl sulfoxide; at 20 ℃; for 20h; pH=8; Reagent/catalyst; Enzymatic reaction;
DOI:10.1002/anie.201601056

Reference yield:

: 108-98-5
thiophenol

: 18922-55-9
S-(n-propyl)-S-phenyl-N-(p-tolylsulfonyl)sulfimide

Guidance literature:: Multi-step reaction with 2 steps

1.1: sodium hydroxide / ethanol / 2 h / 20 °C

1.2: 12 h / 20 °C

2.1: iron(III) tris(4-chloro-2,6-dimethyl-3,5-heptanedionate); 2,6-bis[(4R)-5,5-dihydro-4-phenyl-2-oxazolyl]pyridine / acetone / 16 h / -20 °C

With iron(III) tris(4-chloro-2,6-dimethyl-3,5-heptanedionate); 2,6-bis[(4R)-5,5-dihydro-4-phenyl-2-oxazolyl]pyridine; sodium hydroxide; In ethanol; acetone;
DOI:10.1002/anie.201304451