3H-Imidazo(4,5-f)quinoxalin-2-amine, 3,5,7,8-tetramethyl-

Base Information

Chemical Name:3H-Imidazo(4,5-f)quinoxalin-2-amine, 3,5,7,8-tetramethyl-
CAS No.:146177-58-4
Molecular Formula:C₁₃H₁₅N₅
Molecular Weight:241.296
Hs Code.:
DSSTox Substance ID:DTXSID20163282
Nikkaji Number:J535.180D
Wikidata:Q83032167
Mol file:146177-58-4.mol

Synonyms:146177-58-4;3H-Imidazo(4,5-f)quinoxalin-2-amine, 3,5,7,8-tetramethyl-;3,5,7,8-tetramethylimidazo[4,5-f]quinoxalin-2-amine;2-Amino-3,5,7,8-tetramethylimidazo(4,5-f)quinoxaline;CCRIS 6410;5,7,8-Trimethyl-IQX;2-AMINO-3,5,7,8-TETRAMETHYLIMIDAZO[4,5-F]QUINOXALINE;3,5,7,8-Tetramethyl-3H-imidazo(4,5-f)quinoxalin-2-amine;DTXSID20163282

Suppliers and Price of 3H-Imidazo(4,5-f)quinoxalin-2-amine, 3,5,7,8-tetramethyl-

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
2-AMINO-3,5,7,8-TETRAMETHYLIMIDAZO(4,5-F)QUINOXALINE 95.00%
5MG
$ 499.83

Total 1 raw suppliers

Chemical Property of 3H-Imidazo(4,5-f)quinoxalin-2-amine, 3,5,7,8-tetramethyl-

Chemical Property:

Vapor Pressure:6.76E-09mmHg at 25°C
Boiling Point:467°Cat760mmHg
Flash Point:236.2°C
PSA：70.35000
Density:1.38g/cm³
LogP:1.95400
XLogP3:1.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:0
Exact Mass:241.13274550
Heavy Atom Count:18
Complexity:323

Purity/Quality:: 2-AMINO-3,5,7,8-TETRAMETHYLIMIDAZO(4,5-F)QUINOXALINE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC2=C(C3=NC(=C(N=C13)C)C)N=C(N2C)N

Technology Process of 3H-Imidazo(4,5-f)quinoxalin-2-amine, 3,5,7,8-tetramethyl-

There total 4 articles about 3H-Imidazo(4,5-f)quinoxalin-2-amine, 3,5,7,8-tetramethyl- 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:

: 109671-53-6
7-methyl-5-methylamino-4-nitro-2,1,3-benzoselenadiazole

: 146177-58-4
2-amino-3,5,7,8-tetramethyl-3H-imidazo<4,5-f>quinoxaline

Guidance literature:: Multi-step reaction with 4 steps

1: 71 percent / 40percent aq. NH₄SH / methanol / 3 h / Heating

2: 91 percent / aq. ethanol / 3 h / Heating

3: H₂ / Raney nickel / aq. ethanol / 1 h / Ambient temperature

4: aq. ethanol / 5 °C

With ammonium sulfide; hydrogen; nickel; In methanol; ethanol;

Reference yield:

: 149703-57-1
6-methyl-4-methylamino-3-nitro-1,2-benzenediamine

: 146177-58-4
2-amino-3,5,7,8-tetramethyl-3H-imidazo<4,5-f>quinoxaline

Guidance literature:: Multi-step reaction with 3 steps

1: 91 percent / aq. ethanol / 3 h / Heating

2: H₂ / Raney nickel / aq. ethanol / 1 h / Ambient temperature

3: aq. ethanol / 5 °C

With hydrogen; nickel; In ethanol;

Reference yield:

: 149703-62-8
2,3,8-trimethyl-6-methylamino-5-nitroquinoxaline

: 146177-58-4
2-amino-3,5,7,8-tetramethyl-3H-imidazo<4,5-f>quinoxaline

Guidance literature:: Multi-step reaction with 2 steps

1: H₂ / Raney nickel / aq. ethanol / 1 h / Ambient temperature

2: aq. ethanol / 5 °C

With hydrogen; nickel; In ethanol;