2,4(1H,3H)-Quinolinedione, 3-(butylamino)-3-phenyl-

Base Information

Chemical Name:2,4(1H,3H)-Quinolinedione, 3-(butylamino)-3-phenyl-
CAS No.:477950-04-2
Molecular Formula:C19H20N2O2
Molecular Weight:308.38
Hs Code.:
DSSTox Substance ID:DTXSID80476300
Mol file:477950-04-2.mol

Synonyms:477950-04-2;2,4(1H,3H)-Quinolinedione, 3-(butylamino)-3-phenyl-;DTXSID80476300

Suppliers and Price of 2,4(1H,3H)-Quinolinedione, 3-(butylamino)-3-phenyl-

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of 2,4(1H,3H)-Quinolinedione, 3-(butylamino)-3-phenyl-

Chemical Property:

XLogP3:3.2
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:5
Exact Mass:308.152477885
Heavy Atom Count:23
Complexity:445

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCNC1(C(=O)C2=CC=CC=C2NC1=O)C3=CC=CC=C3

Technology Process of 2,4(1H,3H)-Quinolinedione, 3-(butylamino)-3-phenyl-

There total 2 articles about 2,4(1H,3H)-Quinolinedione, 3-(butylamino)-3-phenyl- 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: 55.0%

: 144603-32-7
3-chloro-3-phenylquinoline-2,4(1H,3H)-dione

: 109-73-9,85404-21-3
N-butylamine

: 477950-04-2
3-butylamino-3-phenylquinoline-2,4-(1H,3H)-dione

Guidance literature:: In N,N-dimethyl-formamide; at 20 ℃; for 24h;
DOI:10.3987/com-02-9522

Reference yield:

: 14933-29-0
4-hydroxy-3-phenyl-2(1H)-quinolone

: 477950-04-2
3-butylamino-3-phenylquinoline-2,4-(1H,3H)-dione

Guidance literature:: Multi-step reaction with 2 steps

1: 89 percent / sulfuryl chloride / dioxane / 0.17 h / 50 - 55 °C

2: 55 percent / dimethylformamide / 24 h / 20 °C

With sulfuryl dichloride; In 1,4-dioxane; N,N-dimethyl-formamide;
DOI:10.3987/com-02-9522