3-Butyl-2-phenyl-4-quinolinecarboxylic acid

Base Information

Chemical Name:3-Butyl-2-phenyl-4-quinolinecarboxylic acid
CAS No.:224633-10-7
Molecular Formula:C₂₀H₁₉NO₂
Molecular Weight:305.376
Hs Code.:
DSSTox Substance ID:DTXSID301260117

Synonyms:DTXSID301260117;3-Butyl-2-phenyl-4-quinolinecarboxylic acid;224633-10-7

Suppliers and Price of 3-Butyl-2-phenyl-4-quinolinecarboxylic acid

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 3-Butyl-2-phenyl-4-quinolinecarboxylic acid

Chemical Property:

XLogP3:5.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:5
Exact Mass:305.141578849
Heavy Atom Count:23
Complexity:391

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCCCC1=C(C2=CC=CC=C2N=C1C3=CC=CC=C3)C(=O)O

Technology Process of 3-Butyl-2-phenyl-4-quinolinecarboxylic acid

There total 1 articles about 3-Butyl-2-phenyl-4-quinolinecarboxylic acid 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:

: 942-92-7
caprophenone

: 91-56-5,1186480-61-4,84788-92-1
indole-2,3-dione

: 224633-10-7
3-butyl-2-phenyl-quinoline-4-carboxylic acid

Guidance literature:: DOI:10.1021/ja01160a047

Reference yield:

: 224633-10-7
3-butyl-2-phenyl-quinoline-4-carboxylic acid

: 3-butyl-2-phenyl-quinoline-4-carbonyl chloride

Guidance literature:: With oxalyl dichloride; In dichloromethane; at 5 - 20 ℃;
DOI:10.1021/jm980633c

Reference yield:

: 224633-10-7
3-butyl-2-phenyl-quinoline-4-carboxylic acid

: (R,S)-N-(α-ethylbenzyl)-3-n-butyl-2-phenylquinoline-4-carboxamide

Guidance literature:: Multi-step reaction with 2 steps

1: (COCl)2 / CH₂Cl₂ / 5 - 20 °C

2: K₂CO₃ / dimethylformamide / 24 h / Ambient temperature

With oxalyl dichloride; potassium carbonate; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jm980633c