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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, 3,4,8-trimethyl-

Cc1cnc2c(n1)c1nc(n(c1c(c2)C)C)N Request for Quotation
Chemical Name: 3H-Imidazo[4,5-f]quinoxalin-2-amine, 3,4,8-trimethyl-
CAS Number: 95896-78-9
Product Number: AG005WK0(AGN-PC-07A1QN)
Synonyms:
MDL No: MFCD00269903
Molecular Formula: C12H13N5
Molecular Weight: 227.2651

Identification/Properties

Properties
MP:
>254°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


As a professional chemist, I can tell you that 3,4,8-Trimethyl-3H-imidazo[4,5-f]quinoxalin-2-amine is a valuable compound utilized in chemical synthesis for its unique structural properties. This compound serves as a versatile building block in the creation of various pharmaceuticals, agrochemicals, and materials. Its distinctive molecular structure makes it an ideal precursor in the development of novel drug candidates and functional materials. In chemical synthesis, 3,4,8-Trimethyl-3H-imidazo[4,5-f]quinoxalin-2-amine can undergo a variety of reactions to introduce functional groups, thereby allowing chemists to tailor its properties for specific applications. Additionally, the presence of multiple methyl groups in the molecule enhances its reactivity and offers opportunities for derivatization, enabling the synthesis of diverse molecular scaffolds. This compound's compatibility with a wide range of synthetic methodologies makes it a valuable tool for researchers in the field of organic chemistry seeking to access structurally complex molecules for various purposes.