4-methyl-N-[methyl(4-methylphenyl)-lambda~4~-sulfanylidene]benzenesulfonamide

Base Information

Chemical Name:4-methyl-N-[methyl(4-methylphenyl)-lambda~4~-sulfanylidene]benzenesulfonamide
CAS No.:24702-26-9
Molecular Formula:C₁₅H₁₇NO₂S₂
Molecular Weight:307.437
Hs Code.:
NSC Number:131876
Mol file:24702-26-9.mol

Synonyms:4-methyl-N-[methyl(4-methylphenyl)-lambda~4~-sulfanylidene]benzenesulfonamide;24702-26-9;(NE)-4-methyl-N-[methyl-(4-methylphenyl)-lambda4-sulfanylidene]benzenesulfonamide;NSC131876;MLS000539678;SCHEMBL17015173;HZTFMTGJVKQSNS-UHFFFAOYSA-N;HMS2300E11;NSC-131876;SMR000162008;AG-803/12478027

Suppliers and Price of 4-methyl-N-[methyl(4-methylphenyl)-lambda~4~-sulfanylidene]benzenesulfonamide

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
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price

Total 1 raw suppliers

Chemical Property of 4-methyl-N-[methyl(4-methylphenyl)-lambda~4~-sulfanylidene]benzenesulfonamide

Chemical Property:

Vapor Pressure:6.62E-09mmHg at 25°C
Boiling Point:479.9°C at 760 mmHg
Flash Point:244°C
Density:1.22g/cm³
XLogP3:4.8
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:3
Exact Mass:307.07007113
Heavy Atom Count:20
Complexity:437

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC=C(C=C1)S(=NS(=O)(=O)C2=CC=C(C=C2)C)C
Isomeric SMILES:CC1=CC=C(C=C1)/S(=N/S(=O)(=O)C2=CC=C(C=C2)C)/C

Technology Process of 4-methyl-N-[methyl(4-methylphenyl)-lambda~4~-sulfanylidene]benzenesulfonamide

There total 23 articles about 4-methyl-N-[methyl(4-methylphenyl)-lambda~4~-sulfanylidene]benzenesulfonamide 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: 99.0%

: 623-13-2
4-methylphenyl methylsulfide

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

: 24702-26-9,37831-86-0,4235-12-5
(S)-S-methyl-S-(4-tolyl)-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 26h; enantioselective reaction;
DOI:10.1002/anie.201304451

Reference yield: 98.0%

: 623-13-2
4-methylphenyl methylsulfide

: 127-65-1
chloroamine-T

: 24702-26-9,37831-86-0,4235-12-5
S-p-Tolyl-S-methyl-N-p-tosylsulfimid

Guidance literature:: In acetonitrile; at 20 ℃; for 16h;
DOI:10.1021/jo0012039

Reference yield: 95.0%

: 941-55-9
4-toluenesulfonyl azide

: 623-13-2
4-methylphenyl methylsulfide

: 24702-26-9,37831-86-0,4235-12-5
S-p-Tolyl-S-methyl-N-p-tosylsulfimid

Guidance literature:: With (5,10,15,20-tetrakis(pentafluorophenyl)porphyrinato)iron(III) chloride; In 1,2-dichloro-ethane; for 24h; Molecular sieve; Inert atmosphere; Reflux;
DOI:10.1002/chem.201000581