CAS 4179-37-7

2-(1,3-Benzodioxol-5-yl)-4-methoxyquinoline

Description:

2-(1,3-Benzodioxol-5-yl)-4-methoxyquinoline, with the CAS number 4179-37-7, is a chemical compound that belongs to the class of quinoline derivatives. This substance features a quinoline core, which is a bicyclic structure composed of a benzene ring fused to a pyridine ring, and is substituted with a methoxy group and a benzodioxole moiety. The presence of the benzodioxole group contributes to its potential biological activity, as this structure is often associated with various pharmacological properties. The compound is typically characterized by its moderate solubility in organic solvents and limited solubility in water, which is common for many organic compounds with complex structures. Its molecular structure suggests potential applications in medicinal chemistry, particularly in the development of compounds with antimicrobial, anti-inflammatory, or anticancer properties. However, specific biological activities and toxicological profiles would require further investigation through experimental studies.

Formula: C₁₇H₁₃NO₃

InChI: InChI=1S/C17H13NO3/c1-19-16-9-14(18-13-5-3-2-4-12(13)16)11-6-7-15-17(8-11)21-10-20-15/h2-9H,10H2,1H3

InChI key: InChIKey=QGCORDIPOBZNKC-UHFFFAOYSA-N

SMILES: O(C)C=1C2=C(N=C(C1)C=3C=C4C(=CC3)OCO4)C=CC=C2

Synonyms:

• 2-(1,3-Benzodioxol-5-yl)-4-methoxyquinoline
• Graveolinine
• Quinoline, 4-methoxy-2-[3,4-(methylenedioxy)phenyl]-
• Quinoline,4-methoxy-2-[3,4-(methylenedioxy)phenyl]- (6CI,7CI,8CI)
• Quinoline, 2-(1,3-benzodioxol-5-yl)-4-methoxy-

Graveolinine

CAS: 4179-37-7

Graveolinine is a quinoline alkaloid that can be isolated from Ruta chalepensis. It exhibits antiplatelet activity by reducing platelet aggregation induced by Arachidonic Acid and Collagen in rabbits.

Formula: C₁₇H₁₃NO₃

Color and Shape: Solid

Molecular weight: 279.29

Ref: TM-TN8452