3-Butyn-1-ol, 4-phenyl- is an organic compound characterized by its alkyne functional group and an alcohol group. It features a butynyl chain, which consists of four carbon atoms with a triple bond between the first and second carbon atoms, and a hydroxyl (-OH) group attached to the terminal carbon. The presence of a phenyl group, which is a benzene ring, at the fourth carbon adds to its complexity and can influence its reactivity and physical properties. This compound is typically a colorless to pale yellow liquid and is soluble in organic solvents. Its structure allows for potential applications in organic synthesis, particularly in the production of more complex molecules. The presence of both the alkyne and alcohol functional groups suggests that it may participate in various chemical reactions, including nucleophilic additions and coupling reactions. As with many organic compounds, safety precautions should be taken when handling it, as it may pose health risks or environmental hazards.

3-Butyn-1-ol, 4-phenyl-

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4-Phenyl-3-butyn-1-ol

4-Phenylbut-3-yn-1-ol is a chiral molecule with two stereogenic centers. It is an intermediate in the synthesis of indenes, which are used as pharmaceuticals and pesticides. 4-Phenylbut-3-yn-1-ol can be prepared by reacting diethyl etherate with acetaldehyde and malonate, or by reacting methylethylketone with ethylene oxide and carbon monoxide. The molecule has intramolecular hydrogen bonding due to the electron withdrawing effect of the carbonyl group on the adjacent phenyl ring. This allows for conformation changes that lead to catalytic activity.

CAS 10229-11-5: 3-Butyn-1-ol, 4-phenyl-

3-Butyn-1-ol, 4-phenyl-

Ref: IN-DA00074K

4-Phenyl-3-butyn-1-ol

Ref: 10-F607519

4-Phenyl-3-butyn-1-ol

Ref: 54-OR77234

4-Phenylbut-3-yn-1-ol

Ref: 3D-KAA22911