(R)-(-)-4-Phenyl-2-butanol is an organic compound characterized by its chiral structure, which includes a phenyl group attached to a butanol backbone. This compound is a secondary alcohol, meaning it has a hydroxyl (-OH) group attached to a carbon that is connected to two other carbon atoms. 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 at room temperature and has a distinctive odor. The compound is known for its applications in organic synthesis and as a chiral building block in pharmaceuticals and agrochemicals. Its chirality is significant in determining its biological activity, as different enantiomers can exhibit different effects in biological systems. Additionally, (R)-(-)-4-Phenyl-2-butanol can participate in various chemical reactions, including oxidation and esterification, making it a versatile compound in synthetic organic chemistry. Safety data should be consulted for handling and storage, as with all chemical substances.

(R)-(-)-4-Phenyl-2-butanol

39516-03-5: (R)-(-)-4-Phenyl-2-butanol is an organic compound characterized by its chiral structure, which includes a phenyl group attached to a butanol backbone. This compound is a secondary alcohol, meaning it has a hydroxyl (-OH) group attached to a carbon that is connected to two other carbon atoms. 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 at room temperature and has a distinctive odor. The compound is known for its applications in organic synthesis and as a chiral building block in pharmaceuticals and agrochemicals. Its chirality is significant in determining its biological activity, as different enantiomers can exhibit different effects in biological systems. Additionally, (R)-(-)-4-Phenyl-2-butanol can participate in various chemical reactions, including oxidation and esterification, making it a versatile compound in synthetic organic chemistry. Safety data should be consulted for handling and storage, as with all chemical substances.

CAS 39516-03-5

(R)-(-)-4-Phenyl-2-butanol

(R)-4-Phenylbutan-2-ol

Ref: IN-DA003C38

(R)-(-)-4-Phenylbutan-2-ol

Ref: 54-OR304056

(R)-4-Phenylbutan-2-ol

Ref: 10-F623924