CAS 1160263-15-9: 6-Chloro-2-(2,5-dimethylphenyl)-4-quinolinecarbonyl chloride

Description: 6-Chloro-2-(2,5-dimethylphenyl)-4-quinolinecarbonyl chloride is a chemical compound characterized by its unique structure, which includes a quinoline moiety and a chloro substituent. This compound features a carbonyl chloride functional group, making it a reactive acyl chloride, which can participate in various chemical reactions, particularly acylation. The presence of the 2,5-dimethylphenyl group contributes to its hydrophobic characteristics, potentially influencing its solubility and reactivity in organic solvents. The chloro group can enhance electrophilicity, making it useful in synthetic organic chemistry for the introduction of acyl groups into other molecules. Additionally, the quinoline structure is known for its biological activity, which may suggest potential applications in pharmaceuticals or agrochemicals. Overall, this compound's reactivity, structural features, and potential applications make it of interest in both research and industrial contexts. However, safety precautions should be observed due to the presence of reactive functional groups.

Formula: C₁₈H₁₃Cl₂NO

InChI: InChI=1S/C18H13Cl2NO/c1-10-3-4-11(2)13(7-10)17-9-15(18(20)22)14-8-12(19)5-6-16(14)21-17/h3-9H,1-2H3

InChI key: InChIKey=LWZACAPKZLDXKI-UHFFFAOYSA-N

SMILES: O=C(Cl)C1=CC(=NC=2C=CC(Cl)=CC21)C=3C=C(C=CC3C)C

Synonyms:

• 4-Quinolinecarbonyl chloride, 6-chloro-2-(2,5-dimethylphenyl)-
• 6-Chloro-2-(2,5-dimethylphenyl)-4-quinolinecarbonyl chloride

6-chloro-2-(2,5-dimethylphenyl)quinoline-4-carbonyl chloride

CAS: 1160263-15-9

• Molecular weight: 330.2099914550781

6-Chloro-2-(2,5-dimethylphenyl)quinoline-4-carbonyl chloride

CAS: 1160263-15-9

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• Formula: C₁₈H₁₃Cl₂NO
• Purity: Min. 95%
• Molecular weight: 330.21 g/mol