Ethyl-(R)-(E)-4,5-O-isopropylidene 4,5-dihydroxypent-2-enoate is a chemical compound characterized by its unique structure, which includes an ethyl ester functional group and a dihydroxypent-2-enoate backbone. The presence of the isopropylidene group indicates that it has a protective acetal structure, which can influence its reactivity and stability. This compound is likely to exhibit chirality due to the (R) configuration, which can affect its biological activity and interactions. The (E) designation refers to the configuration of the double bond in the pent-2-enoate moiety, indicating that the highest priority substituents on either side of the double bond are on opposite sides, which can impact its geometric isomerism. In terms of solubility, it is expected to be soluble in organic solvents due to its ester and hydroxy groups, while its reactivity may include participation in esterification and other nucleophilic reactions. Overall, this compound may have applications in organic synthesis and potentially in pharmaceutical development, depending on its biological properties.

ethyl-(R)-(E)-4,5-O-isopropylidene 4,5-dihydroxypent-2-enoate

104321-62-2: Ethyl-(R)-(E)-4,5-O-isopropylidene 4,5-dihydroxypent-2-enoate is a chemical compound characterized by its unique structure, which includes an ethyl ester functional group and a dihydroxypent-2-enoate backbone. The presence of the isopropylidene group indicates that it has a protective acetal structure, which can influence its reactivity and stability. This compound is likely to exhibit chirality due to the (R) configuration, which can affect its biological activity and interactions. The (E) designation refers to the configuration of the double bond in the pent-2-enoate moiety, indicating that the highest priority substituents on either side of the double bond are on opposite sides, which can impact its geometric isomerism. In terms of solubility, it is expected to be soluble in organic solvents due to its ester and hydroxy groups, while its reactivity may include participation in esterification and other nucleophilic reactions. Overall, this compound may have applications in organic synthesis and potentially in pharmaceutical development, depending on its biological properties.

CAS 104321-62-2

ethyl-(R)-(E)-4,5-O-isopropylidene 4,5-dihydroxypent-2-enoate

Ethyl (R)-()-3-(2,2-dimethyl-1,3-dioxolan-4-yl)-trans-2-propenoate

Ref: IN-DA003PZN