5-Ethynylpyridine-2-carbaldehyde is an organic compound characterized by its pyridine ring, which is a six-membered aromatic heterocycle containing one nitrogen atom. The presence of an ethynyl group (–C≡C–) at the 5-position of the pyridine ring introduces a triple bond, contributing to its reactivity and potential applications in organic synthesis. The aldehyde functional group (–CHO) at the 2-position provides the compound with distinct chemical properties, including the ability to undergo nucleophilic addition reactions and participate in condensation reactions. This compound is typically used in the synthesis of various pharmaceuticals, agrochemicals, and other fine chemicals due to its versatile reactivity. Additionally, its structure allows for potential interactions in coordination chemistry, making it of interest in the development of metal-organic frameworks or catalysts. As with many organic compounds, handling should be done with care, considering potential toxicity and reactivity.

5-ethynylpyridine-2-carbaldehyde

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5-ETHYNYLPICOLINALDEHYDE

5-Ethynylpicolinaldehyde is a nucleotide analogue that has potent anticancer activity. It binds to the DNA double helix and inhibits the replication of DNA by inhibiting the enzyme DNA polymerase. This drug also interacts with drug molecules, which may be due to its supramolecular chemistry. 5-Ethynylpicolinaldehyde has been shown to have excellent anticancer activity in both in vivo and in vitro studies.

CAS 940911-03-5: 5-ethynylpyridine-2-carbaldehyde

5-ETHYNYLPICOLINALDEHYDE

Ref: 10-F301535

5-ethynylpyridine-2-carbaldehyde

Ref: IN-DA00IHXQ

5-Ethynylpicolinaldehyde

Ref: 3D-QMB91103

5-Ethynylpyridine-2-carbaldehyde

Ref: 54-OR77955

5-Ethynylpicolinaldehyde

Ref: TR-E939350