[1,2,4]triazolo[1,5-a]quinoxalin-4(5H)-one

Base Information

Chemical Name:[1,2,4]triazolo[1,5-a]quinoxalin-4(5H)-one
CAS No.:150454-83-4
Molecular Formula:C₉H₆N₄O
Molecular Weight:186.173
Hs Code.:
DSSTox Substance ID:DTXSID10435607
Nikkaji Number:J506.943B
Wikidata:Q82250654
ChEMBL ID:CHEMBL365930
Mol file:150454-83-4.mol

Synonyms:150454-83-4;[1,2,4]triazolo[1,5-a]quinoxalin-4(5H)-one;5H-[1,2,4]TRIAZOLO[1,5-A]QUINOXALIN-4-ONE;[1,2,4]Triazolo[1,5-a]quinoxalin-4-ol;[1,2,4]Triazolo[1,5-a]quinoxalin-4(5H)-one(9CI);D00HVX;CHEMBL365930;DTXSID10435607;PD178529;[1,2,4]Triazolo[1,5-a]quinoxaline-4(5H)-one

Suppliers and Price of [1,2,4]triazolo[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

AccelPharmtech
[1,2,4]Triazolo[1,5-a]quinoxalin-4(5H)-one 97.00%
25G
$ 9900.00

AccelPharmtech
[1,2,4]Triazolo[1,5-a]quinoxalin-4(5H)-one 97.00%
5G
$ 5270.00

Total 1 raw suppliers

Chemical Property of [1,2,4]triazolo[1,5-a]quinoxalin-4(5H)-one

Chemical Property:

PSA：63.05000
LogP:0.57080
XLogP3:0.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:0
Exact Mass:186.05416083
Heavy Atom Count:14
Complexity:257

Purity/Quality:: [1,2,4]Triazolo[1,5-a]quinoxalin-4(5H)-one 97.00% ^*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=NC=NN23

Technology Process of [1,2,4]triazolo[1,5-a]quinoxalin-4(5H)-one

There total 5 articles about [1,2,4]triazolo[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: 75.0%

: 150454-82-3
4,5-dihydro-4-oxo-1,2,4-triazolo<1,5-a>quinoxaline-2-carboxylic acid

: 150454-83-4
4,5-dihydro-1,2,4-triazolo<1,5-a>quinoxalin-4-one

Guidance literature:: With copper(I) oxide; In diethylene glycol; at 135 ℃; for 13h;

Reference yield:

: 114098-35-0
amino-(2-nitro-phenylhydrazono)-acetic acid ethyl ester

: 150454-83-4
4,5-dihydro-1,2,4-triazolo<1,5-a>quinoxalin-4-one

Guidance literature:: Multi-step reaction with 4 steps

1: 12 percent / triethylamine / benzene / 8 h

2: 70 percent / iron (powder), glacial acetic acid / 1 h / 90 °C

3: 90 percent / 0.6M aq. sodium hydroxide / ethanol / 3 h / Heating

4: 75 percent / cuprous oxide / bis-(2-hydroxy-ethyl) ether / 13 h / 135 °C

With copper(I) oxide; sodium hydroxide; iron; acetic acid; triethylamine; In ethanol; diethylene glycol; benzene;

Reference yield:

: 150454-80-1
diethyl 1-(2-nitrophenyl)-1,2,4-triazole-3,5-dicarboxylate

: 150454-83-4
4,5-dihydro-1,2,4-triazolo<1,5-a>quinoxalin-4-one

Guidance literature:: Multi-step reaction with 3 steps

1: 70 percent / iron (powder), glacial acetic acid / 1 h / 90 °C

2: 90 percent / 0.6M aq. sodium hydroxide / ethanol / 3 h / Heating

3: 75 percent / cuprous oxide / bis-(2-hydroxy-ethyl) ether / 13 h / 135 °C

With copper(I) oxide; sodium hydroxide; iron; acetic acid; In ethanol; diethylene glycol;