CAS 52939-12-5

7H-Furo[3,2-g][1]benzopyran-7-one,4-(2-hydroxy-3-methoxy-3-methylbutoxy)-, (R)-

Description:

7H-Furo[3,2-g][1]benzopyran-7-one, 4-(2-hydroxy-3-methoxy-3-methylbutoxy)-, (R)-, with CAS number 52939-12-5, is a complex organic compound characterized by its fused ring structure, which includes a furan and benzopyran moiety. This compound features a hydroxyl group and a methoxy group, contributing to its potential solubility and reactivity. The presence of the 3-methylbutoxy side chain enhances its hydrophobic characteristics, which may influence its biological activity and interaction with other molecules. As a chiral compound, it exists in an (R)-configuration, which can affect its pharmacological properties and interactions with biological systems. Such compounds are often studied for their potential applications in pharmaceuticals, particularly in the development of drugs with specific therapeutic effects. The structural complexity and functional groups present in this molecule suggest it may exhibit interesting chemical behavior, including potential antioxidant or anti-inflammatory properties, although specific biological activities would require further investigation.

Formula: C₁₇H₁₈O₆

(+)-Oxypeucedanin methanolate

CAS: 52939-12-5

(+)-Oxypeucedanin methanolate (compound 9) is a natural compound that inhibits prostaglandin E2 production [1].

Formula: C₁₇H₁₈O₆

Color and Shape: Solid

Molecular weight: 318.32

Ref: TM-T75620

Oxypeucedanin methanolate

CAS: 52939-12-5

Formula: C₁₇H₁₈O₆

Purity: 95%~99%

Molecular weight: 318.325

Ref: BP-BP5087

Oxypeucedanin methanolate

CAS: 52939-12-5

Oxypeucedanin methanolate is a naturally occurring furanocoumarin, which is a type of organic compound found predominantly in several citrus plants. This compound is derived from the peels and essential oils of these plants, highlighting its botanical source that is rich in phytochemicals.

Formula: C₁₇H₁₈O₆

Purity: Min. 95%

Molecular weight: 318.32 g/mol

Ref: 3D-XO163800