N-(5-chloro-2-methylphenyl)-4-methylbenzenesulfonamide

Base Information

Chemical Name:N-(5-chloro-2-methylphenyl)-4-methylbenzenesulfonamide
CAS No.:55816-01-8
Molecular Formula:C14H14ClNO2S
Molecular Weight:295.79
Hs Code.:
DSSTox Substance ID:DTXSID80356118
Wikidata:Q82135292

Synonyms:55816-01-8;N-(5-chloro-2-methylphenyl)-4-methylbenzenesulfonamide;N-(5-chloro-2-methylphenyl)-4-methyl-Benzenesulfonamide;DTXSID80356118;N-(5-Chloro-2-methyl-phenyl)-4-methyl-benzenesulfonamide;MFCD00684398;STL416396;AKOS000383119;SB82459;AS-71455;CS-0313480;W18785;Z45712726;N-(5-chloro-2-methylphenyl)-4-methylbenzene-1-sulfonamide;N-?(5-?chloro-?2-?methylphenyl)?-?4-?methyl-Benzenesulfonamide

Suppliers and Price of N-(5-chloro-2-methylphenyl)-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

AK Scientific
N-a€?(5-a€?chloro-a€?2-a€?methylphenyl)a€?-a€?4-a€?methyl-Benzenesulfonamide
100mg
$ 131.60

Total 2 raw suppliers

Chemical Property of N-(5-chloro-2-methylphenyl)-4-methylbenzenesulfonamide

Chemical Property:

PSA：54.55000
LogP:4.91140
XLogP3:3.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:295.0433776
Heavy Atom Count:19
Complexity:385

Purity/Quality:

99% ^*data from raw suppliers

N-a€?(5-a€?chloro-a€?2-a€?methylphenyl)a€?-a€?4-a€?methyl-Benzenesulfonamide ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC=C(C=C1)S(=O)(=O)NC2=C(C=CC(=C2)Cl)C

Technology Process of N-(5-chloro-2-methylphenyl)-4-methylbenzenesulfonamide

There total 1 articles about N-(5-chloro-2-methylphenyl)-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:

: 98-59-9
p-toluenesulfonyl chloride

: 95-79-4
5-chloro-2-methyl-benzenamine

: 55816-01-8
toluene-4-sulfonic acid-(5-chloro-2-methyl-anilide)

Guidance literature:

Reference yield: 95.0%

: 55816-01-8
toluene-4-sulfonic acid-(5-chloro-2-methyl-anilide)

: 2048-31-9,66820-54-0
(Z)-2-bromo-3-phenylprop-2-en-1-ol

: N-[(Z)-2-bromo-3-phenylprop-2-enyl]-N-(5-chloro-2-methylphenyl)-4-methylbenzenesulfonamide

Guidance literature:: With triphenylphosphine; diethylazodicarboxylate; In toluene; at 0 - 20 ℃; for 1h;
DOI:10.1002/chem.201103819

Reference yield:

: 55816-01-8
toluene-4-sulfonic acid-(5-chloro-2-methyl-anilide)

: 13852-51-2
5-chloro-2-methyl-4-nitroaniline

Guidance literature:: Multi-step reaction with 2 steps

1: water; toluene; HNO₃

2: aqueous H₂SO₄

With sulfuric acid; water; nitric acid; toluene;