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CAS 18159-24-5

:

1H-Pyrrole-2-carboxaldehyde, 1-(phenylmethyl)-

Description:
1H-Pyrrole-2-carboxaldehyde, 1-(phenylmethyl)-, also known by its CAS number 18159-24-5, is an organic compound characterized by the presence of a pyrrole ring, which is a five-membered aromatic heterocycle containing nitrogen. This compound features a carboxaldehyde functional group (-CHO) at the 2-position of the pyrrole ring and a benzyl group (phenylmethyl) at the 1-position. It is typically a colorless to pale yellow liquid or solid, depending on its purity and specific conditions. The presence of both the aldehyde and the aromatic benzyl group contributes to its reactivity, making it useful in various synthetic applications, including the production of pharmaceuticals and agrochemicals. The compound may exhibit properties such as solubility in organic solvents and potential biological activity, which can be explored in medicinal chemistry. Safety data should be consulted for handling and storage, as with all chemical substances, to ensure proper precautions are taken.
Formula:C12H11NO
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Found 4 products.
  • 1-benzylpyrrole-2-carbaldehyde

    CAS:
    Formula:C12H11NO
    Molecular weight:185.2218

    Ref: IN-DA0022YR

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  • 1-Benzylpyrrole-2-carbaldehyde

    CAS:
    <p>1-Benzylpyrrole-2-carbaldehyde</p>
    Purity:95%
    Molecular weight:185.22g/mol

    Ref: 54-OR910391

    1g
    920.00€
    250mg
    360.00€
  • 1-BENZYL-1H-PYRROLE-2-CARBALDEHYDE

    CAS:
    Formula:C12H11NO
    Purity:95.0%
    Color and Shape:Liquid
    Molecular weight:185.226

    Ref: 10-F334038

    1g
    1,123.00€
    250mg
    471.00€
  • 1-Benzyl-1H-pyrrole-2-carbaldehyde

    CAS:
    <p>1-Benzyl-1H-pyrrole-2-carbaldehyde is a chemical compound that yields 1,4-benzodioxan-6,7(2H)-dione as an intermediate. The β-cyclodextrin is used to increase the solubility of the product. The shift in the UV spectrum of 1,4-benzodioxan-6,7(2H)-dione in the presence of 1-[(β-cyclodextrin)amino]ethyl methide was mediated by azafulvenium (1) and pyridine (3). This reaction was found to be intramolecular and n-substituted. Azafulvenium (1) activated the carbonyl group of 1-(N′N′dimethylaminoethyl methide) at position 6 on the pyrrole ring by hypervalent interaction with nitrogen. This reagent can be used for synthesis</p>
    Formula:C12H11NO
    Purity:Min. 95%
    Molecular weight:185.23 g/mol

    Ref: 3D-TAA15924

    1g
    725.00€
    100mg
    344.00€