N-Mesitylbenzenesulfonamide

Base Information

Chemical Name:N-Mesitylbenzenesulfonamide
CAS No.:16939-28-9
Molecular Formula:C15H17NO2S
Molecular Weight:275.366
Hs Code.:2935009090
NSC Number:86739
DSSTox Substance ID:DTXSID40937629
Nikkaji Number:J3.425.358G
Wikidata:Q82913841
ChEMBL ID:CHEMBL2131154
Mol file:16939-28-9.mol

Synonyms:N-Mesitylbenzenesulfonamide;n-(2,4,6-trimethylphenyl)benzenesulfonamide;16939-28-9;MLS002694708;CHEMBL2131154;N-(2,4,6-TriMethylphenyl)benzenesulfonaMide, 97per cent;NSC86739;starbld0015411;Cambridge id 5112615;NCIOpen2_004872;SCHEMBL812686;DTXSID40937629;HMS3080D10;BDBM50044899;MFCD00541882;NSC-86739;STL419879;AKOS003979961;SMR001560631;CS-0333896;AH-034/04668016

Suppliers and Price of N-Mesitylbenzenesulfonamide

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

American Custom Chemicals Corporation
N-(2,4,6-TRIMETHYLPHENYL)BENZENESULFONAMIDE 95.00%
5MG
$ 495.10

Total 5 raw suppliers

Chemical Property of N-Mesitylbenzenesulfonamide

Chemical Property:

Vapor Pressure:8.6E-07mmHg at 25°C
Boiling Point:405.7°C at 760 mmHg
PKA:9.48±0.10(Predicted)
Flash Point:199.2°C
PSA：54.55000
Density:1.211g/cm³
LogP:4.56640
XLogP3:3.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:275.09799996
Heavy Atom Count:19
Complexity:369

Purity/Quality:

99% ^*data from raw suppliers

N-(2,4,6-TRIMETHYLPHENYL)BENZENESULFONAMIDE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC(=C(C(=C1)C)NS(=O)(=O)C2=CC=CC=C2)C

Technology Process of N-Mesitylbenzenesulfonamide

There total 3 articles about N-Mesitylbenzenesulfonamide 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:

: 938-10-3
phenylsulfonyl azide

: 108-67-8
1,3,5-trimethyl-benzene

: 16939-28-9
N-(2,4,6-trimethylphenyl)benzenesulfonamide

Guidance literature:: In neat (no solvent); at 130 ℃; for 12h; Inert atmosphere; Sealed tube; Green chemistry;
DOI:10.1016/j.tetlet.2015.02.009

Reference yield:

: 98-09-9
benzenesulfonyl chloride

: 16939-28-9
N-(2,4,6-trimethylphenyl)benzenesulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: sodium azide / water; acetone / 12 h / 0 - 20 °C

2: neat (no solvent) / 12 h / 130 °C / Inert atmosphere; Sealed tube; Green chemistry

With sodium azide; In water; acetone;
DOI:10.1016/j.tetlet.2015.02.009