CAS 502925-47-5
:6-(4-Methoxyphenyl)-2-pyridinecarboxaldehyde
Description:
6-(4-Methoxyphenyl)-2-pyridinecarboxaldehyde, identified by its CAS number 502925-47-5, is an organic compound characterized by its pyridine and aldehyde functional groups. This compound features a pyridine ring substituted at the 2-position with a carboxaldehyde group and at the 6-position with a 4-methoxyphenyl group, which contributes to its aromatic properties. The presence of the methoxy group enhances its lipophilicity and can influence its reactivity and interactions with biological systems. Typically, compounds like this may exhibit interesting biological activities, making them potential candidates for pharmaceutical applications. The molecular structure allows for various chemical reactions, including nucleophilic additions and condensation reactions, due to the electrophilic nature of the aldehyde group. Additionally, the compound's solubility and stability can vary depending on the solvent and environmental conditions. Overall, 6-(4-Methoxyphenyl)-2-pyridinecarboxaldehyde is a versatile compound with potential applications in organic synthesis and medicinal chemistry.
Formula:C13H11NO2
InChI:InChI=1S/C13H11NO2/c1-16-12-7-5-10(6-8-12)13-4-2-3-11(9-15)14-13/h2-9H,1H3
InChI key:InChIKey=JLUDQJVIZSPJFQ-UHFFFAOYSA-N
SMILES:C(=O)C1=NC(=CC=C1)C2=CC=C(OC)C=C2
Synonyms:- 2-Pyridinecarboxaldehyde, 6-(4-methoxyphenyl)-
- 6-(4-Methoxyphenyl)-2-pyridinecarboxaldehyde
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Found 5 products.
6-(4-(Methylamino)phenyl)picolinaldehyde
CAS:Formula:C13H11NO2Purity:98%Color and Shape:SolidMolecular weight:213.23196-(4-Methoxyphenyl)Picolinaldehyde
CAS:6-(4-Methoxyphenyl)PicolinaldehydePurity:99%Molecular weight:213.23g/mol6-(4-(METHYLAMINO)PHENYL)PICOLINALDEHYDE
CAS:Formula:C13H12N2OPurity:97.0%Color and Shape:SolidMolecular weight:212.2526-(4-Methoxyphenyl)pyridine-2-carbaldehyde
CAS:<p>6-(4-Methoxyphenyl)pyridine-2-carbaldehyde (6MPCA) is a ligand that can be used in catalytic reactions. It has been shown to be a high-activity catalyst for the carbonylation of levulinic acid. 6MPCA also catalyzes the transfer hydrogenation of vanillyl alcohol and other alcohols, with high activity. Furfural was found to be an effective substrate for this reaction.</p>Formula:C13H11NO2Purity:Min. 95%Molecular weight:213.23 g/mol



