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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)-

Quinoxaline, 6,7-dimethyl-2-phenyl-

Cc1cc2ncc(nc2cc1C)c1ccccc1 Request for Quotation
Chemical Name: Quinoxaline, 6,7-dimethyl-2-phenyl-
CAS Number: 71897-07-9
Product Number: AG005P7S(AGN-PC-0JK63R)
Synonyms:
MDL No:
Molecular Formula: C16H14N2
Molecular Weight: 234.2958

Identification/Properties

Properties
MP:
127-129°C
Storage:
2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
234.302g/mol
XLogP3:
3.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
234.116g/mol
Monoisotopic Mass:
234.116g/mol
Topological Polar Surface Area:
25.8A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
272
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


6,7-Dimethyl-2-phenylquinoxaline is a versatile compound widely used in chemical synthesis due to its unique structural properties. This compound serves as a valuable building block in the preparation of various organic molecules, especially in the development of pharmaceuticals, agrochemicals, and materials science. Its compact and rigid structure makes it an ideal candidate for creating complex aromatic frameworks with enhanced stability and reactivity. In organic synthesis, 6,7-Dimethyl-2-phenylquinoxaline can act as a key intermediate in the synthesis of biologically active compounds, such as anticancer agents, antimicrobial agents, and fluorescent dyes. By incorporating this compound into the molecular design, chemists can fine-tune the physicochemical properties of the final products for specific applications in the field of medicinal chemistry and materials research.