4(3H)-Quinazolinone, 3-butyl-

Base Information

Chemical Name:4(3H)-Quinazolinone, 3-butyl-
CAS No.:16417-02-0
Molecular Formula:C12H14 N2 O
Molecular Weight:202.256
Hs Code.:
DSSTox Substance ID:DTXSID70167715
Nikkaji Number:J73.052A
Wikidata:Q83037147

Synonyms:3-Butyl-4(3H)-quinazolinone;4(3H)-Quinazolinone, 3-butyl-;BRN 0147718;16417-02-0;4-Quinazolone, 3-butyl;5-24-03-00027 (Beilstein Handbook Reference);3-Butylquinazolin-4(3H)-one;DTXSID70167715;3-butyl-3,4-dihydroquinazolin-4-one;LS-140444;FT-0733914

Suppliers and Price of 4(3H)-Quinazolinone, 3-butyl-

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
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price

Total 1 raw suppliers

Chemical Property of 4(3H)-Quinazolinone, 3-butyl-

Chemical Property:

Vapor Pressure:0.000115mmHg at 25°C
Boiling Point:336°Cat760mmHg
Flash Point:157°C
Density:1.11g/cm³
XLogP3:1.9
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:202.110613074
Heavy Atom Count:15
Complexity:262

Purity/Quality:: 98%min ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCN1C=NC2=CC=CC=C2C1=O

Technology Process of 4(3H)-Quinazolinone, 3-butyl-

There total 1 articles about 4(3H)-Quinazolinone, 3-butyl- 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%

: 83-34-1
3-Methylindole

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

: 16417-02-0
N³-n-butylquinazolin-4-one

Guidance literature:: With tert.-butylhydroperoxide; tetra-(n-butyl)ammonium iodide; In water; acetonitrile; at 100 ℃; for 12h; Schlenk technique; Inert atmosphere;
DOI:10.1021/acs.orglett.0c00271