2-Amino-3,4,7-trimethylimidazo(4,5-f)quinoxaline

Base Information

Chemical Name:2-Amino-3,4,7-trimethylimidazo(4,5-f)quinoxaline
CAS No.:97389-17-8
Molecular Formula:C₁₂H₁₃N₅
Molecular Weight:227.269
Hs Code.:2933990090
UNII:88RJ219WYW
DSSTox Substance ID:DTXSID10242914
Nikkaji Number:J456.404I
Wikidata:Q27894168
Mol file:97389-17-8.mol

Synonyms:97389-17-8;2-Amino-3,4,7-trimethylimidazo(4,5-f)quinoxaline;8-Demethyl-4,7-dimethyl meiqx;3,4,7-trimethyl-3h-imidazo[4,5-f]quinoxalin-2-amine;3,4,7-Trimethyl-3H-imidazo(4,5-f)quinoxalin-2-amine;3H-Imidazo(4,5-f)quinoxalin-2-amine, 3,4,7-trimethyl-;88RJ219WYW;4,7-Dimethyl-IQX;4,7-DIMEIQX;CCRIS 6403;BRN 5344701;2-AMINO-3,4,7-TRIMETHYLIMIDAZO[4,5-F]QUINOXALINE;UNII-88RJ219WYW;DTXSID10242914;Q27894168

Suppliers and Price of 2-Amino-3,4,7-trimethylimidazo(4,5-f)quinoxaline

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

American Custom Chemicals Corporation
3,4,7-TRIMETHYL-3H-IMIDAZO(4,5-F)QUINOXALIN-2-AMINE 95.00%
5MG
$ 505.36

Total 5 raw suppliers

Chemical Property of 2-Amino-3,4,7-trimethylimidazo(4,5-f)quinoxaline

Chemical Property:

Vapor Pressure:6.77E-09mmHg at 25°C
Boiling Point:467°Cat760mmHg
Flash Point:236.2°C
PSA：69.62000
Density:1.42g/cm³
LogP:2.29670
XLogP3:1.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:0
Exact Mass:227.11709544
Heavy Atom Count:17
Complexity:297

Purity/Quality:

97% ^*data from raw suppliers

3,4,7-TRIMETHYL-3H-IMIDAZO(4,5-F)QUINOXALIN-2-AMINE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC2=NC(=CN=C2C3=C1N(C(=N3)N)C)C

Technology Process of 2-Amino-3,4,7-trimethylimidazo(4,5-f)quinoxaline

There total 10 articles about 2-Amino-3,4,7-trimethylimidazo(4,5-f)quinoxaline 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: 62.0%

: 138336-32-0
2-(N-benzylamino)-3,4,7-trimethylimidazo<4,5-f>quinoxaline

: 97389-17-8
3,4,7-trimethyl-3H-imidazo<4,5-f>quinoxalin-2-amine

Guidance literature:: With ammonium formate; palladium on activated charcoal; In methanol; for 168h; Heating;
DOI:10.1021/jo00031a017

Reference yield:

: 138336-20-6
2-(methylthio)-3,4,7-trimethylimidazo<4,5-f>quinoxaline

: 97389-17-8
3,4,7-trimethyl-3H-imidazo<4,5-f>quinoxalin-2-amine

Guidance literature:: Multi-step reaction with 3 steps

1: 82.4 percent / aq. KMnO₄, glacial acetic acid / 1 h / Ambient temperature

2: 99.4 percent / 168 h / 140 - 150 °C

3: 62 percent / ammonium formate / 10percent Pd/C / methanol / 168 h / Heating

With potassium permanganate; ammonium formate; acetic acid; palladium on activated charcoal; In methanol;
DOI:10.1021/jo00031a017

Reference yield:

: 138336-26-2
2-(methylsulfonyl)-3,4,7-trimethylimidazo<4,5-f>quinoxaline

: 97389-17-8
3,4,7-trimethyl-3H-imidazo<4,5-f>quinoxalin-2-amine

Guidance literature:: Multi-step reaction with 2 steps

1: 99.4 percent / 168 h / 140 - 150 °C

2: 62 percent / ammonium formate / 10percent Pd/C / methanol / 168 h / Heating

With ammonium formate; palladium on activated charcoal; In methanol;
DOI:10.1021/jo00031a017