2,3-dichloro-6,7-dimethylquinoxaline
$200.00
CAS No.: 63810-80-0
Catalog No.: WLZ1590
Purity: 95%
MF: C10H8Cl2N2
MW: 227.094
Storage: 2-8 degree Celsius
SMILES: ClC1=NC2=CC(=C(C=C2N=C1Cl)C)C
Catalog No.: WLZ1590
Purity: 95%
MF: C10H8Cl2N2
MW: 227.094
Storage: 2-8 degree Celsius
SMILES: ClC1=NC2=CC(=C(C=C2N=C1Cl)C)C
CAS NO.: 63810-80-0; 2,3-dichloro-6,7-dimethylquinoxaline. PROPERTIES: This heterocyclic compound features two chlorine atoms and two methyl groups on a quinoxaline ring, creating a molecule with potential applications in organic synthesis and pharmaceutical research. The 2,3-dichloro-6,7-dimethylquinoxaline typically appears as a white crystalline powder with moderate solubility in common organic solvents. Its molecular structure includes electron-withdrawing chlorine atoms and electron-donating methyl groups that influence the electronic properties of the quinoxaline system. For optimal stability and to prevent degradation, this compound should be stored at 2-8 degree Celsius in a tightly sealed container under anhydrous conditions. When handling, appropriate safety measures including nitrile gloves and safety goggles are essential. This compound is sensitive to moisture and may hydrolyze in aqueous environments. In case of accidental spillage, clean the area with a damp cloth and dispose of materials according to local regulations. APPLICATIONS: The 2,3-dichloro-6,7-dimethylquinoxaline serves as a valuable intermediate in the synthesis of quinoxaline-containing bioactive molecules and materials with specific electronic properties. The chlorine substituents provide handles for further functionalization through nucleophilic substitution reactions. In medicinal chemistry, this compound functions as a building block for developing pharmaceuticals targeting enzyme inhibitors and receptor modulators. The quinoxaline ring contributes to target binding affinity and selectivity. Additionally, the molecule finds utility in materials science as a monomer for creating polymers with specific electronic and optical properties. Researchers utilizing this compound benefit from its defined halogenation pattern and functional group arrangement, enabling the development of advanced materials with tailored electronic characteristics.
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