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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

3H-Imidazo[4,5-f]quinoxalin-2-amine, 3,7,8-trimethyl-

Cc1nc2c(nc1C)ccc1c2nc(n1C)N Request for Quotation
Chemical Name: 3H-Imidazo[4,5-f]quinoxalin-2-amine, 3,7,8-trimethyl-
CAS Number: 92180-79-5
Product Number: AG00631O(AGN-PC-07A1QO)
Synonyms:
MDL No:
Molecular Formula: C12H13N5
Molecular Weight: 227.2651

Identification/Properties

Properties
MP:
>294°C (dec.)
Storage:
2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
227.271g/mol
XLogP3:
1.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
0
Exact Mass:
227.117g/mol
Monoisotopic Mass:
227.117g/mol
Topological Polar Surface Area:
69.6A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
297
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Amino-3,7,8-trimethylimidazo[4,5-f]quinoxaline is a versatile compound widely utilized in chemical synthesis for its unique properties and reactivity. This compound serves as a valuable building block in the creation of various pharmaceuticals, agrochemicals, and fine chemicals. Its structural features make it a key intermediate in the synthesis of complex organic molecules, particularly in the formation of heterocyclic compounds.In the realm of chemical synthesis, 2-Amino-3,7,8-trimethylimidazo[4,5-f]quinoxaline plays a crucial role as a precursor for the construction of nitrogen-containing molecules with diverse functionalities. Its amino group allows for selective derivatization, enabling the attachment of different functional groups to tailor the molecular properties for specific applications. Moreover, the trimethylimidazo[4,5-f]quinoxaline moiety imparts structural stability and rigidity to the final compounds, enhancing their bioactivity and overall performance.Researchers and chemists leverage the unique reactivity of 2-Amino-3,7,8-trimethylimidazo[4,5-f]quinoxaline to access novel chemical entities with potential pharmacological or biological relevance. By incorporating this compound into synthetic routes, scientists can efficiently access structurally diverse compounds with tailored properties, paving the way for the development of new drug candidates, agrochemicals, and advanced materials.Overall, the application of 2-Amino-3,7,8-trimethylimidazo[4,5-f]quinoxaline in chemical synthesis underscores its significance as a valuable tool for expanding the chemical space and unlocking new opportunities for molecular design and discovery.