N-2-biphenylyl-4-methylbenzenesulfonamide

Base Information

Chemical Name:N-2-biphenylyl-4-methylbenzenesulfonamide
CAS No.:24310-30-3
Molecular Formula:C19H17NO2S
Molecular Weight:323.415
Hs Code.:2935009090
DSSTox Substance ID:DTXSID20355968
Nikkaji Number:J111.583I
Wikidata:Q82135070
Pharos Ligand ID:JK7M9QGC4VUP
ChEMBL ID:CHEMBL1382128
Mol file:24310-30-3.mol

Synonyms:MLS000575428;N-2-biphenylyl-4-methylbenzenesulfonamide;SMR000184678;N-Biphenyl-2-yl-4-methyl-benzenesulfonamide;N-{[1,1'-biphenyl]-2-yl}-4-methylbenzene-1-sulfonamide;24310-30-3;N-tosyl-2-aminobiphenyl;4-methyl-N-(2-phenylphenyl)benzenesulfonamide;Cambridge id 5182458;Oprea1_088899;Oprea1_411098;cid_818647;SCHEMBL2516997;CHEMBL1382128;BDBM46912;DTXSID20355968;VPIDANAIZIMNGX-UHFFFAOYSA-N;HMS2379F09;STK016133;AKOS001095547;N-(biphenyl-2-yl)-4-methylbenzenesulfonamide;EN300-18163997;N-[1,1'-biphenyl]-2-yl-4-methylbenzenesulfonamide;SR-01000690192-2;Z45702226

Suppliers and Price of N-2-biphenylyl-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 3 raw suppliers

Chemical Property of N-2-biphenylyl-4-methylbenzenesulfonamide

Chemical Property:

PSA：54.55000
LogP:5.61660
XLogP3:4.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:323.09799996
Heavy Atom Count:23
Complexity:456

Purity/Quality:: 99% ^*data from raw 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=CC=CC=C2C3=CC=CC=C3

Technology Process of N-2-biphenylyl-4-methylbenzenesulfonamide

There total 9 articles about N-2-biphenylyl-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: 100.0%

: 90-41-5
2-phenylaniline

: 98-59-9
p-toluenesulfonyl chloride

: 24310-30-3
N-biphenyl-2-yl-4-methylbenzenesulfonamide

Guidance literature:: With triethylamine; In dichloromethane; at 4 ℃;
DOI:10.1002/adsc.201800824

Reference yield:

: 98-80-6
phenylboronic acid

: 24310-30-3
N-biphenyl-2-yl-4-methylbenzenesulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate; bis-triphenylphosphine-palladium(II) chloride / N,N-dimethyl-formamide; water / 24 h / 80 °C / Inert atmosphere

2: pyridine / 2 h / 120 °C

With pyridine; bis-triphenylphosphine-palladium(II) chloride; potassium carbonate; In water; N,N-dimethyl-formamide;
DOI:10.1021/ol4001922