4-methyl-N-quinolin-3-ylbenzenesulfonamide

Base Information

Chemical Name:4-methyl-N-quinolin-3-ylbenzenesulfonamide
CAS No.:7101-92-0
Molecular Formula:C₁₆H₁₄N₂O₂S
Molecular Weight:298.365
Hs Code.:
DSSTox Substance ID:DTXSID801271747
Nikkaji Number:J3.579.761K
ChEMBL ID:CHEMBL1299349

Synonyms:4-methyl-N-quinolin-3-ylbenzenesulfonamide;4-Methyl-N-3-quinolinylbenzenesulfonamide;4-Methyl-N-(3-quinolinyl)benzenesulfonamide;Benzenesulfonamide, 4-methyl-N-3-quinolinyl-;MLS-0090809.0001;7101-92-0;3-tosylaminoquinoline;N-Tosyl-3-quinolineamine;4-Methyl-N-quinolin-3-yl-benzenesulfonamide;Oprea1_712648;Oprea1_871009;CBDivE_004710;MLS000714768;cid_588682;CHEMBL1299349;BDBM45792;DTXSID801271747;HMS2670J18;STK831995;AKOS000621475;SMR000274747;4-methyl-N-(3-quinolyl)benzenesulfonamide;4-methyl-N-(quinolin-3-yl)benzenesulfonamide;J3.579.761K;4-Methyl-N-(3-quinolinyl)benzenesulfonamide #;Benzenesulfonamide, 4-methyl-N-(3-quinolinyl)-;AG-205/03194021;SR-01000509738;SR-01000509738-1;BRD-K10166560-001-07-9;Z237649678

Suppliers and Price of 4-methyl-N-quinolin-3-ylbenzenesulfonamide

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 0 raw suppliers

Chemical Property of 4-methyl-N-quinolin-3-ylbenzenesulfonamide

Chemical Property:

XLogP3:3.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:3
Exact Mass:298.07759887
Heavy Atom Count:21
Complexity:438

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1=CC=C(C=C1)S(=O)(=O)NC2=CC3=CC=CC=C3N=C2

Technology Process of 4-methyl-N-quinolin-3-ylbenzenesulfonamide

There total 2 articles about 4-methyl-N-quinolin-3-ylbenzenesulfonamide 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: 78.0%

: 580-17-6
3-aminoquinoline

: 98-59-9
p-toluenesulfonyl chloride

: 7101-92-0
N-(quinolin-3-yl)-4-methylbenzenesulfonamide

Guidance literature:: With pyridine; for 1h; Ambient temperature;
DOI:10.3987/COM-92-5999

Reference yield:

: 7101-92-0
N-(quinolin-3-yl)-4-methylbenzenesulfonamide

Guidance literature:: 3-Aminochinolin, p-Toluol-sulfonylchlorid;

Reference yield: 96.0%

: 7101-92-0
N-(quinolin-3-yl)-4-methylbenzenesulfonamide

: (R)-N-(1,2,3,4-tetrahydroquinolin-3-yl)-4-methylbenzenesulfonamide

Guidance literature:: With (S)-3,3'-bis(triphenylsilyl)-1,1'-binaphthyl-2,2'-diyl hydrogenphosphate; diethyl 2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate; In benzene; at 50 ℃; for 48h; Solvent; Temperature; enantioselective reaction; Catalytic behavior; Schlenk technique; Inert atmosphere;
DOI:10.1039/c6nj02249a