CAS 22280-95-1
:3-methoxy-4-(prop-2-en-1-yloxy)benzaldehyde
Description:
3-Methoxy-4-(prop-2-en-1-yloxy)benzaldehyde, with the CAS number 22280-95-1, is an organic compound characterized by its aromatic structure, which includes a methoxy group and an allyloxy substituent on a benzaldehyde framework. This compound features a benzene ring with a formyl group (-CHO) and a methoxy group (-OCH3) at the 3-position, while the 4-position is substituted with a prop-2-en-1-yloxy group, which introduces a double bond and contributes to its reactivity. The presence of the aldehyde functional group indicates that it can participate in various chemical reactions, such as nucleophilic addition and condensation reactions. Additionally, the methoxy group enhances the compound's solubility in organic solvents and may influence its electronic properties, making it a potential candidate for applications in organic synthesis and materials science. Its unique structure may also impart specific biological activities, warranting further investigation in medicinal chemistry.
Formula:C11H12O3
InChI:InChI=1/C11H12O3/c1-3-6-14-10-5-4-9(8-12)7-11(10)13-2/h3-5,7-8H,1,6H2,2H3
SMILES:C=CCOc1ccc(cc1OC)C=O
Synonyms:- 4-(Allyloxy)-3-Methoxybenzaldehyde
- Benzaldehyde, 3-Methoxy-4-(2-Propen-1-Yloxy)-
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Found 4 products.
4-(Allyloxy)-3-methoxybenzaldehyde
CAS:4-(Allyloxy)-3-methoxybenzaldehydePurity:≥95%Molecular weight:192.21118g/mol4-(allyloxy)-3-methoxybenzaldehyde
CAS:Formula:C11H12O3Purity:98%Color and Shape:Liquid, No data available.Molecular weight:192.214O-allylvanillin
CAS:<p>O-Allylvanillin, an O-allylchalcone derivative, exhibits anti-cancer properties by inhibiting the growth of THP-1, HL60, Hep-G2, and MCF-7 cells with IC50 values of 74.76 μM, 63.52 μM, 90.99 μM, and 90.11 μM, respectively [1].</p>Formula:C11H12O3Purity:98%Color and Shape:SolidMolecular weight:192.21



