Imidazo[1,5-a]quinoxalin-4(5H)-one

Base Information

Chemical Name:Imidazo[1,5-a]quinoxalin-4(5H)-one
CAS No.:179042-26-3
Molecular Formula:C₁₀H₇N₃O
Molecular Weight:185.185
Hs Code.:2933990090
DSSTox Substance ID:DTXSID60573341
Nikkaji Number:J1.528.654G
Wikidata:Q82462040
Mol file:179042-26-3.mol

Synonyms:Imidazo[1,5-a]quinoxalin-4(5H)-one;179042-26-3;4H,5H-imidazo[1,5-a]quinoxalin-4-one;5H-IMIDAZO[1,5-A]QUINOXALIN-4-ONE;Imidazo[1,5-a]quinoxalin-4(5H)-one (9CI);MLS004734601;SCHEMBL4763948;DTXSID60573341;imidazo[1,5-a]quinoxalin-4-one;AKOS022188713;SB74941;SMR003484535;CS-0308156;EN300-109925;Z1216855542

Suppliers and Price of Imidazo[1,5-a]quinoxalin-4(5H)-one

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

Crysdot
Imidazo[1,5-a]quinoxalin-4(5H)-one 95+%
1g
$ 491.00

Alichem
Imidazo[1,5-a]quinoxalin-4(5H)-one
1g
$ 401.00

AK Scientific
Imidazo[1,5-a]quinoxalin-4(5H)-one
250mg
$ 567.00

AccelPharmtech
Imidazo[1,5-a]quinoxalin-4(5H)-one 97.00%
25G
$ 6000.00

AccelPharmtech
Imidazo[1,5-a]quinoxalin-4(5H)-one 97.00%
5G
$ 3230.00

Total 5 raw suppliers

Chemical Property of Imidazo[1,5-a]quinoxalin-4(5H)-one

Chemical Property:

PSA：50.42000
LogP:1.58810
Storage Temp.:2-8°C
XLogP3:0.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:0
Exact Mass:185.058911855
Heavy Atom Count:14
Complexity:256

Purity/Quality:

97% ^*data from raw suppliers

Imidazo[1,5-a]quinoxalin-4(5H)-one 95+% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C2C(=C1)NC(=O)C3=CN=CN23

Technology Process of Imidazo[1,5-a]quinoxalin-4(5H)-one

There total 7 articles about Imidazo[1,5-a]quinoxalin-4(5H)-one 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: 97.0%

: 221025-37-2
5-(4-methoxybenzyl)imidazo[1,5-a]quinoxalin-4(5H)-one

: 179042-26-3
imidazo[1,5-a]quinoxalin-6(5H)-one

Guidance literature:: With trifluorormethanesulfonic acid; methoxybenzene; trifluoroacetic acid; at 20 ℃;
DOI:10.1016/S0040-4039(01)00697-9

Reference yield: 95.0%

: N-(2-fluoroanilino)-1H-imidazole-4-carboxamide

: 179042-26-3
imidazo[1,5-a]quinoxalin-6(5H)-one

Guidance literature:: With sodium hydride; In N,N-dimethyl acetamide; for 48h; Reflux;
DOI:10.1016/j.ejmech.2017.07.021

Reference yield:

: C₁₅H₂₀N₂O₄

: 38622-91-2,36635-61-7
[(p-methylphenyl)sulfonylmethyl]isonitrile

: 179042-26-3
imidazo[1,5-a]quinoxalin-6(5H)-one

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; toluene; at 180 ℃; for 0.166667h; Temperature; Time; Microwave irradiation;
DOI:10.1016/j.tetlet.2012.08.072