1H-Imidazo(4,5-c)quinoline-2,4-dione, 3,5-dihydro-5-butyl-1-methyl-

Base Information

Chemical Name:1H-Imidazo(4,5-c)quinoline-2,4-dione, 3,5-dihydro-5-butyl-1-methyl-
CAS No.:133306-21-5
Molecular Formula:C₁₅H₁₇N₃O₂
Molecular Weight:271.319
Hs Code.:
DSSTox Substance ID:DTXSID70158067
Nikkaji Number:J515.275E
Wikidata:Q83026224
ChEMBL ID:CHEMBL131067

Synonyms:BRN 5821142;133306-21-5;1H-Imidazo(4,5-c)quinoline-2,4-dione, 3,5-dihydro-5-butyl-1-methyl-;3,5-Dihydro-5-butyl-1-methyl-1H-imidazo(4,5-c)quinoline-2,4-dione;CHEMBL131067;SCHEMBL9206737;DTXSID70158067;LS-80499;1-Methyl-2-hydroxy-5-butyl-1H-imidazo[4,5-c]quinolin-4(5H)-one

Suppliers and Price of 1H-Imidazo(4,5-c)quinoline-2,4-dione, 3,5-dihydro-5-butyl-1-methyl-

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 1 raw suppliers

Chemical Property of 1H-Imidazo(4,5-c)quinoline-2,4-dione, 3,5-dihydro-5-butyl-1-methyl-

Chemical Property:

Boiling Point:°Cat760mmHg
Flash Point:°C
Density:1.3g/cm³
XLogP3:1.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:271.132076794
Heavy Atom Count:20
Complexity:472

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCN1C2=CC=CC=C2C3=C(C1=O)NC(=O)N3C

Technology Process of 1H-Imidazo(4,5-c)quinoline-2,4-dione, 3,5-dihydro-5-butyl-1-methyl-

There total 6 articles about 1H-Imidazo(4,5-c)quinoline-2,4-dione, 3,5-dihydro-5-butyl-1-methyl- 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:

: 5-n-Butyl-7-chloro-1-methyl-1H,5H-imidazo[4,5-c]quinolin-4-one hydrochloride

: 133306-21-5
5-butyl-2-hydroxy-1-methyl-1H-imidazo<4,5-c>quinolin-4(5H)-one

Guidance literature:: With 1,1'-carbonyldiimidazole; carbon palladium; In tetrahydrofuran; ethanol;

Reference yield:

: 392323-50-1
1-butyl-4-hydroxy-3-nitroquinolin-2(1H)-one

: 133306-21-5
5-butyl-2-hydroxy-1-methyl-1H-imidazo<4,5-c>quinolin-4(5H)-one

Guidance literature:: Multi-step reaction with 4 steps

1: POCl₃ / 1 h / Heating

2: 85 percent / tetrahydrofuran / 12 h / Ambient temperature

3: H₂ / 10percent Pd/C / ethanol / 4 h / Ambient temperature

4: tetrahydrofuran / 4 h / Heating

With hydrogen; trichlorophosphate; palladium on activated charcoal; In tetrahydrofuran; ethanol;
DOI:10.1021/jm00100a009

Reference yield:

: 133306-31-7
1-butyl-4-chloro-3-nitroquinolin-2(1H)-one

: 133306-21-5
5-butyl-2-hydroxy-1-methyl-1H-imidazo<4,5-c>quinolin-4(5H)-one

Guidance literature:: Multi-step reaction with 3 steps

1: 85 percent / tetrahydrofuran / 12 h / Ambient temperature

2: H₂ / 10percent Pd/C / ethanol / 4 h / Ambient temperature

3: tetrahydrofuran / 4 h / Heating

With hydrogen; palladium on activated charcoal; In tetrahydrofuran; ethanol;
DOI:10.1021/jm00100a009