(R)-(+)-1-Phenyl-1-pentanol is an organic compound characterized by its chiral structure, which includes a phenyl group attached to a pentanol backbone. This compound is a secondary alcohol, featuring a hydroxyl (-OH) group on the first carbon of a five-carbon chain. The presence of the phenyl group contributes to its aromatic characteristics, influencing its solubility and reactivity. It is typically a colorless to pale yellow liquid with a pleasant odor, and it is soluble in organic solvents while having limited solubility in water due to its hydrophobic phenyl group. The compound exhibits optical activity, meaning it can rotate plane-polarized light, a property attributed to its chiral center. (R)-(+)-1-Phenyl-1-pentanol is utilized in various applications, including as a chiral building block in organic synthesis and in the production of pharmaceuticals and fragrances. Its unique properties make it valuable in both industrial and research settings, particularly in the development of enantiomerically pure compounds.

(R)-(+)-1-Phenyl-1-pentanol

19641-53-3: (R)-(+)-1-Phenyl-1-pentanol is an organic compound characterized by its chiral structure, which includes a phenyl group attached to a pentanol backbone. This compound is a secondary alcohol, featuring a hydroxyl (-OH) group on the first carbon of a five-carbon chain. The presence of the phenyl group contributes to its aromatic characteristics, influencing its solubility and reactivity. It is typically a colorless to pale yellow liquid with a pleasant odor, and it is soluble in organic solvents while having limited solubility in water due to its hydrophobic phenyl group. The compound exhibits optical activity, meaning it can rotate plane-polarized light, a property attributed to its chiral center. (R)-(+)-1-Phenyl-1-pentanol is utilized in various applications, including as a chiral building block in organic synthesis and in the production of pharmaceuticals and fragrances. Its unique properties make it valuable in both industrial and research settings, particularly in the development of enantiomerically pure compounds.

CAS 19641-53-3

(R)-(+)-1-Phenyl-1-pentanol

(1R)-1-Phenylpentan-1-ol

Ref: 3D-UAA64153