CAS 514-67-0
:(9aR)-3-hexanoyl-9a-methyl-6-[(1E)-prop-1-en-1-yl]-2H-furo[3,2-g]isochromene-2,9(9aH)-dione
Description:
The chemical substance known as "(9aR)-3-hexanoyl-9a-methyl-6-[(1E)-prop-1-en-1-yl]-2H-furo[3,2-g]isochromene-2,9(9aH)-dione," with the CAS number 514-67-0, is a complex organic compound characterized by its unique structural features. It belongs to the class of isochromenes, which are bicyclic compounds containing a fused furan and benzene ring. This particular compound exhibits a furo[3,2-g]isochromene framework, indicating the presence of a furan moiety fused to an isochromene structure. The presence of a hexanoyl group and a prop-1-en-1-yl substituent contributes to its reactivity and potential biological activity. The stereochemistry at the 9a position, denoted by the (9aR) configuration, suggests specific spatial arrangements that may influence its interactions in biological systems. Such compounds often exhibit diverse pharmacological properties, making them of interest in medicinal chemistry and natural product research. However, detailed studies on its specific properties, such as solubility, stability, and biological activity, would be necessary to fully understand its potential applications.
Formula:C21H22O5
InChI:InChI=1/C21H22O5/c1-4-6-7-9-17(22)18-16-11-13-10-14(8-5-2)25-12-15(13)19(23)21(16,3)26-20(18)24/h5,8,10-12H,4,6-7,9H2,1-3H3/b8-5+/t21-/m1/s1
Synonyms:- (9aR)-3-hexanoyl-9a-methyl-6-[(E)-prop-1-enyl]furo[3,2-g]isochromene-2,9-dione
- Rubropuncatatin
- 2H-Furo[3,2-g][2]benzopyran-2,9(9aH)-dione, 9a-methyl-3-(1-oxohexyl)-6-(1E)-1-propen-1-yl-, (9aR)-
- RUBROPUNCTATIN
- (R)-9a-Methyl-3-(1-oxohexyl)-6-[(E)-1-propenyl]-2H-furo[3,2-g][2]benzopyran-2,9(9aH)-dione
- (R-(E))-9A-Methyl-3-(1-oxohexyl)-6-(1-propenyl)-2H-furo(3,2-G)(2)benzopyran-2,9(9ah)-dione
- 2H-Furo(3,2-G)(2)benzopyran-2,9(9ah)-dione, 9A-methyl-3-(1-oxohexyl)-6-(1-propenyl)-, (R-(E))-
- See more synonyms
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Found 4 products.
Rubropunctatin
CAS:<p>Rubropunctatin is a polyketide compound, which is a secondary metabolite produced by certain fungal species, specifically Monascus. It functions primarily by disrupting cellular processes, exhibiting inhibitory effects on various enzymes, including those involved in cholesterol biosynthesis. Rubropunctatin's mode of action involves the alteration of metabolic pathways, making it a compound of interest in biochemical and pharmacological research.</p>Formula:C21H22O5Purity:Min. 95%Color and Shape:PowderMolecular weight:354.4 g/mol



