The chemical substance known as "2-Propenoic acid, 3-(3,4-dihydroxyphenyl)-,(1R,3R,4R,5R)-1,4-dihydroxy-7-oxo-6-oxabicyclo[3.2.1]oct-3-yl ester," with the CAS number 106357-47-5, is a complex organic compound characterized by its bicyclic structure and multiple functional groups. It features a propenoic acid moiety, which indicates the presence of an unsaturated carboxylic acid, contributing to its reactivity and potential applications in polymer chemistry. The compound also contains a dihydroxyphenyl group, suggesting antioxidant properties and potential biological activity. The stereochemistry, denoted by the (1R,3R,4R,5R) configuration, implies specific spatial arrangements that can influence its interactions and reactivity. The presence of ester linkages indicates that it may participate in esterification reactions, while the oxabicyclo structure suggests unique conformational properties. Overall, this compound's intricate structure and functional groups may render it of interest in various fields, including medicinal chemistry and materials science, although specific applications would depend on further research and characterization.

2-Propenoic acid, 3-(3,4-dihydroxyphenyl)-,(1R,3R,4R,5R)-1,4-dihydroxy-7-oxo-6-oxabicyclo[3.2.1]oct-3-yl ester

106357-47-5: The chemical substance known as "2-Propenoic acid, 3-(3,4-dihydroxyphenyl)-,(1R,3R,4R,5R)-1,4-dihydroxy-7-oxo-6-oxabicyclo[3.2.1]oct-3-yl ester," with the CAS number 106357-47-5, is a complex organic compound characterized by its bicyclic structure and multiple functional groups. It features a propenoic acid moiety, which indicates the presence of an unsaturated carboxylic acid, contributing to its reactivity and potential applications in polymer chemistry. The compound also contains a dihydroxyphenyl group, suggesting antioxidant properties and potential biological activity. The stereochemistry, denoted by the (1R,3R,4R,5R) configuration, implies specific spatial arrangements that can influence its interactions and reactivity. The presence of ester linkages indicates that it may participate in esterification reactions, while the oxabicyclo structure suggests unique conformational properties. Overall, this compound's intricate structure and functional groups may render it of interest in various fields, including medicinal chemistry and materials science, although specific applications would depend on further research and characterization.

<p>3-Caffeoyl-1,5-quinolactone (3-Caffeoyl-gamma-quinide) is a coffee-derived compound, identified as a phytochemical present in roasted coffee beans. It is primarily formed during the roasting process through the complex transformation of caffeoylquinic acids, which are abundant in green coffee beans. This compound is gaining attention for its notable biological properties, particularly its antioxidant and enzyme inhibitory activities.</p>

CAS 106357-47-5

2-Propenoic acid, 3-(3,4-dihydroxyphenyl)-,(1R,3R,4R,5R)-1,4-dihydroxy-7-oxo-6-oxabicyclo[3.2.1]oct-3-yl ester

3-Caffeoyl-1,5-quinolactone(3-Caffeoyl-gamma-quinide)

Ref: 3D-FC165789