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CAS 19301-35-0

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Benzo[b]thiophene-5-ol

Description:
Benzo[b]thiophene-5-ol is an organic compound characterized by its fused ring structure, which includes a benzene ring and a thiophene ring, with a hydroxyl (-OH) group attached at the 5-position of the thiophene. This compound typically exhibits properties associated with both aromatic and heterocyclic compounds, such as stability and potential reactivity due to the presence of the hydroxyl group. It is generally a pale yellow to brown solid at room temperature and may have a characteristic odor. Benzo[b]thiophene-5-ol is soluble in organic solvents but has limited solubility in water, reflecting its hydrophobic nature. The compound is of interest in various fields, including organic synthesis and materials science, due to its potential applications in pharmaceuticals and as a building block for more complex molecules. Its chemical behavior can be influenced by the presence of the hydroxyl group, which can participate in hydrogen bonding and affect its reactivity and interactions with other substances.
Formula:C8H6OS
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Found 4 products.
  • 5-Hydroxythionaphthene

    CAS:
    Formula:C8H6OS
    Purity:98%
    Color and Shape:Solid
    Molecular weight:150.1976

    Ref: IN-DA00AO83

    1g
    200.00€
    5g
    To inquire
    100mg
    67.00€
    250mg
    106.00€
  • Benzo[b]thiophen-5-ol

    CAS:
    Benzo[b]thiophen-5-ol
    Purity:98%
    Molecular weight:150.202g/mol

    Ref: 54-OR72998

    1g
    280.00€
    5g
    1,223.00€
    100mg
    65.00€
    250mg
    97.00€
  • Benzo[b]thiophen-5-ol

    CAS:
    Formula:C8H6OS
    Purity:98%
    Color and Shape:Solid
    Molecular weight:150.2

    Ref: 10-F302879

    1g
    223.00€
    5g
    980.00€
    100mg
    53.00€
    250mg
    80.00€
  • Benzo[b]thiophen-5-ol

    CAS:
    <p>Benzo[b]thiophen-5-ol is a chiral molecule that has been synthesized to be homochiral. It has an active site and selective epoxide hydration activity, which is the rate-limiting step of epoxide ring opening reactions. The mechanism of this reaction is the cleavage of a C–C bond in an epoxide substrate by an O–H or S–H bond in benzo[b]thiophen-5-ol. The nature of this mechanistic bond cleavage reaction is unknown, but it may be due to catalysis by a benzyl group.</p>
    Formula:C8H6OS
    Purity:Min. 95%
    Molecular weight:150.2 g/mol

    Ref: 3D-UAA30135

    1g
    491.00€
    2g
    To inquire
    5g
    1,302.00€
    500mg
    303.00€