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CAS 4924-22-5

:

Acetic acid 1-acetyl-2-(2,3-dihydro-2-phenyl-4H-1-benzopyran-4-ylidene)hydrazide

Description:
Acetic acid 1-acetyl-2-(2,3-dihydro-2-phenyl-4H-1-benzopyran-4-ylidene)hydrazide, with the CAS number 4924-22-5, is a chemical compound that features a hydrazide functional group linked to an acetic acid moiety. This compound is characterized by its complex structure, which includes a benzopyran ring, contributing to its potential biological activity. The presence of the hydrazide group suggests that it may participate in various chemical reactions, such as condensation and hydrazone formation. Additionally, the compound may exhibit properties such as solubility in polar solvents, depending on the specific substituents and their interactions. Its structural features may also indicate potential applications in pharmaceuticals or as a synthetic intermediate in organic chemistry. However, detailed studies would be necessary to fully understand its reactivity, stability, and potential uses in various fields. As with many organic compounds, safety data and handling precautions should be considered when working with this substance.
Formula:C19H18N2O3
InChI:InChI=1S/C19H18N2O3/c1-13(22)21(14(2)23)20-17-12-19(15-8-4-3-5-9-15)24-18-11-7-6-10-16(17)18/h3-11,19H,12H2,1-2H3
InChI key:InChIKey=UNGWSRDLOLQJGX-UHFFFAOYSA-N
SMILES:N(N(C(C)=O)C(C)=O)=C1C=2C(OC(C1)C3=CC=CC=C3)=CC=CC2
Synonyms:
  • Acetic acid 1-acetyl-2-(2,3-dihydro-2-phenyl-4H-1-benzopyran-4-ylidene)hydrazide
  • Acetic acid, acetyl(2,3-dihydro-2-phenyl-4H-1-benzopyran-4-ylidene)hydrazide
  • Hydrazine, 1,1-diacetyl-2-(2-phenyl-4-chromanylidene)-
  • N-acetyl-N'-(2-phenyl-2,3-dihydro-4H-chromen-4-ylidene)acetohydrazide
  • N-acetyl-N'-[(4E)-2-phenyl-2,3-dihydro-4H-chromen-4-ylidene]acetohydrazide
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Found 1 products.
  • Flavanone diacetyl hydrazone
    Biosynth
    + Info

    Flavanone diacetyl hydrazone

    CAS:
    <p>Flavanone diacetyl hydrazone is a hydrogenated flavonoid derivative, which is synthesized from natural flavonoid sources. This compound exhibits its mode of action primarily through its ability to donate hydrogen atoms, effectively scavenging free radicals and inhibiting oxidative stress. Furthermore, it interacts with various cellular pathways to exert anti-inflammatory effects, making it a potential therapeutic agent in oxidative stress-related disorders.</p>
    Formula:C19H18N2O3
    Purity:Min. 95%
    Molecular weight:322.36 g/mol

    Ref: 3D-FF66604

    10mg
    135.00€
    25mg
    227.00€