CAS 156006-10-9: 3,4-dimethyl-7-(2-oxopropoxy)-2H-chromen-2-one

Description: 3,4-Dimethyl-7-(2-oxopropoxy)-2H-chromen-2-one, with the CAS number 156006-10-9, is a synthetic organic compound belonging to the class of flavonoids, specifically a coumarin derivative. This compound features a chromenone core, characterized by a benzopyran structure, which is substituted at the 3 and 4 positions with methyl groups, enhancing its lipophilicity and potentially influencing its biological activity. The presence of a 2-oxopropoxy group at the 7 position introduces additional functional properties, which may affect solubility and reactivity. Generally, compounds of this nature are studied for their potential pharmacological effects, including antioxidant, anti-inflammatory, and antimicrobial activities. The structural modifications can also influence the compound's interaction with biological targets, making it of interest in medicinal chemistry. As with many flavonoids, the compound may exhibit a range of biological activities, but specific studies would be necessary to elucidate its precise mechanisms and applications.

Formula: C₁₄H₁₄O₄

InChI: InChI=1/C14H14O4/c1-8(15)7-17-11-4-5-12-9(2)10(3)14(16)18-13(12)6-11/h4-6H,7H2,1-3H3

Synonyms:

• 2H-1-benzopyran-2-one, 3,4-dimethyl-7-(2-oxopropoxy)-

2H-1-Benzopyran-2-one, 3,4-dimethyl-7-(2-oxopropoxy)-

CAS: 156006-10-9

• Formula: C₁₄H₁₄O₄
• Molecular weight: 246.2586

3,4-dimethyl-7-(2-oxopropoxy)-2H-chromen-2-one

CAS: 156006-10-9

• Purity: 95.0%
• Molecular weight: 246.26199340820312

3,4-Dimethyl-7-(2-oxopropoxy)-2H-1-benzopyran-2-one

CAS: 156006-10-9

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• Formula: C₁₄H₁₄O₄
• Purity: Min. 95%
• Molecular weight: 246.26 g/mol