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CAS 10229-11-5

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

Description:
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.
Formula:C10H10O
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Found 4 products.
  • 3-Butyn-1-ol, 4-phenyl-

    CAS:
    Formula:C10H10O
    Purity:95%
    Color and Shape:Liquid
    Molecular weight:146.1858

    Ref: IN-DA00074K

    1g
    156.00€
    5g
    571.00€
    100mg
    71.00€
    250mg
    112.00€
  • 4-Phenyl-3-butyn-1-ol

    CAS:
    4-Phenyl-3-butyn-1-ol
    Purity:95%
    Molecular weight:146.19g/mol

    Ref: 54-OR77234

    1g
    264.00€
    5g
    833.00€
    100mg
    72.00€
    250mg
    104.00€
  • 4-Phenyl-3-butyn-1-ol

    CAS:
    Purity:95%
    Molecular weight:146.1889954

    Ref: 10-F607519

    1g
    202.00€
    5g
    625.00€
    100mg
    57.00€
    250mg
    86.00€
  • 4-Phenylbut-3-yn-1-ol

    CAS:
    <p>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.</p>
    Formula:C10H10O
    Purity:Min. 95%
    Molecular weight:146.19 g/mol

    Ref: 3D-KAA22911

    5g
    1,464.00€
    500mg
    410.00€