1-(4-Methylpyridin-2-yl)-1H-pyrrole-2-carbaldehyde, with the CAS number 383136-14-9, is an organic compound characterized by its unique structure that combines a pyrrole ring with a pyridine moiety. This compound features a carbaldehyde functional group, which contributes to its reactivity and potential applications in organic synthesis. The presence of the methyl group on the pyridine ring influences its electronic properties and solubility, making it a versatile intermediate in the synthesis of various pharmaceuticals and agrochemicals. Typically, compounds of this nature exhibit moderate to high polarity due to the presence of both nitrogen-containing heterocycles and the aldehyde group. They may also display interesting biological activities, which can be explored in medicinal chemistry. The compound is likely to be stable under standard conditions but may undergo reactions typical of aldehydes, such as oxidation or condensation. Overall, 1-(4-methylpyridin-2-yl)-1H-pyrrole-2-carbaldehyde represents a valuable structure in the field of organic chemistry, particularly in the development of novel compounds.

1-(4-methylpyridin-2-yl)-1H-pyrrole-2-carbaldehyde

383136-14-9: 1-(4-Methylpyridin-2-yl)-1H-pyrrole-2-carbaldehyde, with the CAS number 383136-14-9, is an organic compound characterized by its unique structure that combines a pyrrole ring with a pyridine moiety. This compound features a carbaldehyde functional group, which contributes to its reactivity and potential applications in organic synthesis. The presence of the methyl group on the pyridine ring influences its electronic properties and solubility, making it a versatile intermediate in the synthesis of various pharmaceuticals and agrochemicals. Typically, compounds of this nature exhibit moderate to high polarity due to the presence of both nitrogen-containing heterocycles and the aldehyde group. They may also display interesting biological activities, which can be explored in medicinal chemistry. The compound is likely to be stable under standard conditions but may undergo reactions typical of aldehydes, such as oxidation or condensation. Overall, 1-(4-methylpyridin-2-yl)-1H-pyrrole-2-carbaldehyde represents a valuable structure in the field of organic chemistry, particularly in the development of novel compounds.

CAS 383136-14-9

1-(4-methylpyridin-2-yl)-1H-pyrrole-2-carbaldehyde

1-(4-methylpyridin-2-yl)-1H-pyrrole-2-carbaldehyde

Ref: IN-DA007AA6

1-(4-Methyl-pyridin-2-yl)-1H-pyrrole-2-carbaldehyde

Ref: 10-F058254