4H-Imidazo(4,5-c)quinolin-4-one, 1,5-dihydro-5-butyl-1-(phenylmethyl)-

Base Information

Chemical Name:4H-Imidazo(4,5-c)quinolin-4-one, 1,5-dihydro-5-butyl-1-(phenylmethyl)-
CAS No.:133305-98-3
Molecular Formula:C₂₁H₂₁N₃O
Molecular Weight:331.417
Hs Code.:
DSSTox Substance ID:DTXSID80158058
Nikkaji Number:J515.270D
Wikidata:Q83026215
ChEMBL ID:CHEMBL128139

Synonyms:1-Benzyl-5-n-butyl-1H,5H-imidazo(4,5-c)quinolin-4-one;4H-Imidazo(4,5-c)quinolin-4-one, 1,5-dihydro-5-butyl-1-(phenylmethyl)-;1,5-Dihydro-5-butyl-1-(phenylmethyl)-4H-imidazo(4,5-c)quinolin-4-one;133305-98-3;CHEMBL128139;SCHEMBL9204643;DTXSID80158058;LS-80467;1-Benzyl-5-butyl-1H-imidazo[4,5-c]quinolin-4(5H)-one

Suppliers and Price of 4H-Imidazo(4,5-c)quinolin-4-one, 1,5-dihydro-5-butyl-1-(phenylmethyl)-

Supply Marketing:

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

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of 4H-Imidazo(4,5-c)quinolin-4-one, 1,5-dihydro-5-butyl-1-(phenylmethyl)-

Chemical Property:

Vapor Pressure:3.85E-13mmHg at 25°C
Boiling Point:573.1°Cat760mmHg
Flash Point:300.4°C
Density:1.18g/cm³
XLogP3:4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:5
Exact Mass:331.168462302
Heavy Atom Count:25
Complexity:462

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCN1C2=CC=CC=C2C3=C(C1=O)N=CN3CC4=CC=CC=C4

Technology Process of 4H-Imidazo(4,5-c)quinolin-4-one, 1,5-dihydro-5-butyl-1-(phenylmethyl)-

There total 3 articles about 4H-Imidazo(4,5-c)quinolin-4-one, 1,5-dihydro-5-butyl-1-(phenylmethyl)- 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:

: 99023-72-0
1-benzyl-1H-imidazo[4,5-c]quinoline

: 133305-98-3
1-Benzyl-5-n-butyl-1H,5H-imidazo[4,5-c]quinolin-4-one

Guidance literature:: Multi-step reaction with 3 steps

1: 30percent aq. H₂O₂ / acetic acid / 12 h / 80 °C

2: acetic anhydride / 1 h / Heating

3: 1.) NaH / 1.) DMF, 50 deg C, 0.5 h, 2.) DMF, 50 deg C, 2 h

With dihydrogen peroxide; acetic anhydride; sodium hydride; In acetic acid;
DOI:10.1021/jm00100a009

Reference yield:

: 99010-49-8
1-Benzyl-1H-imidazo[4,5-c]quinoline 5-oxide

: 133305-98-3
1-Benzyl-5-n-butyl-1H,5H-imidazo[4,5-c]quinolin-4-one

Guidance literature:: Multi-step reaction with 2 steps

1: acetic anhydride / 1 h / Heating

2: 1.) NaH / 1.) DMF, 50 deg C, 0.5 h, 2.) DMF, 50 deg C, 2 h

With acetic anhydride; sodium hydride;
DOI:10.1021/jm00100a009

Reference yield:

: 542-69-8
1-iodo-butane

: 134049-86-8
1-benzyl-4-hydroxy-1H-imidazo<4,5-c>quinoline

: 133305-98-3
1-Benzyl-5-n-butyl-1H,5H-imidazo[4,5-c]quinolin-4-one

Guidance literature:: With sodium hydride; Yield given. Multistep reaction; 1.) DMF, 50 deg C, 0.5 h, 2.) DMF, 50 deg C, 2 h;
DOI:10.1021/jm00100a009