The chemical substance known as "(3aR,5R,6S,6aR)-5-allyl-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-6-ol" with the CAS number 546141-37-1 is characterized by its complex bicyclic structure, which includes a tetrahydrofuran ring fused to a dioxole moiety. This compound features multiple stereocenters, contributing to its chiral nature, which can influence its biological activity and interactions. The presence of an allyl group and two methyl groups on the tetrahydrofuran ring suggests potential reactivity and steric effects that may affect its chemical behavior. The hydroxyl group (–OH) indicates that it is likely to exhibit hydrogen bonding capabilities, which can enhance its solubility in polar solvents and influence its reactivity in various chemical reactions. Overall, this compound's unique structural features may make it of interest in fields such as organic synthesis, medicinal chemistry, and materials science, where its specific properties can be leveraged for various applications.

(3aR,5R,6S,6aR)-5-allyl-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-6-ol

546141-37-1: The chemical substance known as "(3aR,5R,6S,6aR)-5-allyl-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-6-ol" with the CAS number 546141-37-1 is characterized by its complex bicyclic structure, which includes a tetrahydrofuran ring fused to a dioxole moiety. This compound features multiple stereocenters, contributing to its chiral nature, which can influence its biological activity and interactions. The presence of an allyl group and two methyl groups on the tetrahydrofuran ring suggests potential reactivity and steric effects that may affect its chemical behavior. The hydroxyl group (–OH) indicates that it is likely to exhibit hydrogen bonding capabilities, which can enhance its solubility in polar solvents and influence its reactivity in various chemical reactions. Overall, this compound's unique structural features may make it of interest in fields such as organic synthesis, medicinal chemistry, and materials science, where its specific properties can be leveraged for various applications.

<p>5,6,7-Trideoxy-1,2-O-isopropylidene-a-D-xylohept-6enofuranose is a natural homologue of guanine. It is an analog that has been shown to be a mitogen activated protein (MAP) kinase activator in the presence of pyridine. This compound also activates guanosine triphosphatase and has repolarizing effects on cardiac muscle cells. 5,6,7-Trideoxy-1,2-O-isopropylidenea-[D]-xylohept-[6]enofuranose binds to the catalytic site of guanosine triphosphatase and causes a conformational change that results in increased enzyme activity. 5,6,7-Trideoxy-[1]2--isopropylidene--[A]-D--xylohept-[6</p>

CAS 546141-37-1

(3aR,5R,6S,6aR)-5-allyl-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-6-ol

5,6,7-Trideoxy-1,2-O-isopropylidene-a-D-xylo-hept-6-enofuranose

Ref: 3D-MA45377