The chemical substance known as (5S,6S)-5-hydroxy-6-[(1E)-prop-1-en-1-yl]-5,6-dihydro-2H-pyran-2-one, with the CAS number 28921-94-0, is a naturally occurring compound that belongs to the class of pyranones. This compound features a pyran ring, which is a six-membered ring containing one oxygen atom and five carbon atoms, and is characterized by the presence of a hydroxyl group (-OH) and a propenyl substituent. The stereochemistry indicated by the (5S,6S) configuration suggests specific spatial arrangements of the substituents around the chiral centers at positions 5 and 6, which can influence its biological activity and reactivity. This compound may exhibit various properties such as solubility in organic solvents, potential antioxidant activity, and interactions with biological systems, making it of interest in fields like medicinal chemistry and natural product research. Its structural features may also contribute to its role in various biochemical pathways or as a precursor in synthetic organic chemistry.

(5S,6S)-5-hydroxy-6-[(1E)-prop-1-en-1-yl]-5,6-dihydro-2H-pyran-2-one

28921-94-0: The chemical substance known as (5S,6S)-5-hydroxy-6-[(1E)-prop-1-en-1-yl]-5,6-dihydro-2H-pyran-2-one, with the CAS number 28921-94-0, is a naturally occurring compound that belongs to the class of pyranones. This compound features a pyran ring, which is a six-membered ring containing one oxygen atom and five carbon atoms, and is characterized by the presence of a hydroxyl group (-OH) and a propenyl substituent. The stereochemistry indicated by the (5S,6S) configuration suggests specific spatial arrangements of the substituents around the chiral centers at positions 5 and 6, which can influence its biological activity and reactivity. This compound may exhibit various properties such as solubility in organic solvents, potential antioxidant activity, and interactions with biological systems, making it of interest in fields like medicinal chemistry and natural product research. Its structural features may also contribute to its role in various biochemical pathways or as a precursor in synthetic organic chemistry.

CAS 28921-94-0

(5S,6S)-5-hydroxy-6-[(1E)-prop-1-en-1-yl]-5,6-dihydro-2H-pyran-2-one

Phomalactone

Ref: 8R-CL0001

Phomalactone

Ref: 54-BIBR1076