3H-Imidazo(4,5-f)quinoxalin-2-amine, 3,4-dimethyl-

Base Information

Chemical Name:3H-Imidazo(4,5-f)quinoxalin-2-amine, 3,4-dimethyl-
CAS No.:108354-48-9
Molecular Formula:C₁₁H₁₁N₅
Molecular Weight:213.242
Hs Code.:
DSSTox Substance ID:DTXSID20148519
Nikkaji Number:J369.998F
Wikidata:Q83014062
Mol file:108354-48-9.mol

Synonyms:108354-48-9;4-Methyl-iqx;3H-Imidazo(4,5-f)quinoxalin-2-amine, 3,4-dimethyl-;3,4-dimethylimidazo[4,5-f]quinoxalin-2-amine;CCRIS 6402;2-Amino-3,4-dimethylimidazo[4,5-f]quinoxaline;3H-Imidazo[4,5-f]quinoxalin-2-amine,3,4-dimethyl-;2-Amino-3,4-dimethylimidazo(4,5-f)quinoxaline;3,4-Dimethyl-3H-imidazo(4,5-f)quinoxalin-2-amine;3,4-DIMETHYL-3H-IMIDAZO[4,5-F]QUINOXALIN-2-AMINE;DTXSID20148519;LS-80531;2-amino-3,4-dimethyl-imidazo[4,5-f]quinoxaline

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

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

TRC
2-Amino-3,4-dimethylimidazo[4,5-f]quinoxaline
50mg
$ 1320.00

Total 15 raw suppliers

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

Chemical Property:

Vapor Pressure:4.18E-09mmHg at 25°C
Boiling Point:472.7°Cat760mmHg
Flash Point:239.7°C
PSA：70.35000
Density:1.47g/cm³
LogP:1.33720
XLogP3:0.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:0
Exact Mass:213.10144537
Heavy Atom Count:16
Complexity:271

Purity/Quality:

99% ^*data from raw suppliers

2-Amino-3,4-dimethylimidazo[4,5-f]quinoxaline ^*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
Uses 2-Amino-3,4-dimethylimidazo[4,5-f]quinoxaline is used in analytical studies to identify abundant mutagenic heterocyclic aromatic amine that are formed in cooked beef.

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

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

: 63155-04-4
4-chloro-5-methylbenzene-1,2-diamine

: 77500-04-0,108354-48-9
2-amino-3,4-dimethyl-3H-imidazo<4,5-f>quinoxaline

Guidance literature:: Multi-step reaction with 7 steps

1: 88 percent / aq. HCl, SeO₂ / 80 °C

2: 56 percent / conc. H₂SO₄, conc. HNO₃ / 1 h / 0 - 20 °C

3: 82 percent / 2-methoxy-ethanol; H₂O / 0.17 h / Heating

4: 40percent aq. NH₄SH / methanol / 3 h / Heating

5: 51 percent / methanol; H₂O / 3 h / Heating

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

7: aq. ethanol / 5 °C

With hydrogenchloride; selenium(IV) oxide; ammonium sulfide; sulfuric acid; hydrogen; nitric acid; nickel; In methanol; ethanol; 2-methoxy-ethanol; water;

Reference yield:

: 2255-94-9
5-chloro-6-methyl-2,1,3-benzoselenadiazole

: 77500-04-0,108354-48-9
2-amino-3,4-dimethyl-3H-imidazo<4,5-f>quinoxaline

Guidance literature:: Multi-step reaction with 6 steps

1: 56 percent / conc. H₂SO₄, conc. HNO₃ / 1 h / 0 - 20 °C

2: 82 percent / 2-methoxy-ethanol; H₂O / 0.17 h / Heating

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

4: 51 percent / methanol; H₂O / 3 h / Heating

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

6: aq. ethanol / 5 °C

With ammonium sulfide; sulfuric acid; hydrogen; nitric acid; nickel; In methanol; ethanol; 2-methoxy-ethanol; water;

Reference yield:

: 147021-84-9
5-chloro-6-methyl-4-nitro-2,1,3-benzoselenadiazole

: 77500-04-0,108354-48-9
2-amino-3,4-dimethyl-3H-imidazo<4,5-f>quinoxaline

Guidance literature:: Multi-step reaction with 5 steps

1: 82 percent / 2-methoxy-ethanol; H₂O / 0.17 h / Heating

2: 40percent aq. NH₄SH / methanol / 3 h / Heating

3: 51 percent / methanol; H₂O / 3 h / Heating

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

5: aq. ethanol / 5 °C

With ammonium sulfide; hydrogen; nickel; In methanol; ethanol; 2-methoxy-ethanol; water;