2-Chloro-4-(2-furyl)pyrimidine is a heterocyclic organic compound characterized by the presence of a pyrimidine ring substituted with a chlorine atom and a furyl group. The molecular structure features a pyrimidine core, which is a six-membered ring containing two nitrogen atoms at positions 1 and 3, and a chlorine atom at position 2. The furyl group, derived from furan, is attached at position 4 of the pyrimidine ring, contributing to the compound's unique properties. This compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. It is of interest in medicinal chemistry and agricultural applications due to its potential biological activity, including antimicrobial and herbicidal properties. The presence of both the chlorine and furyl substituents can influence the compound's reactivity and interaction with biological targets. Safety data should be consulted for handling and usage, as halogenated compounds can pose environmental and health risks.

2-Chloro-4-(2-furyl)pyrimidine

124959-28-0: 2-Chloro-4-fur-2-ylpyrimidine, 2-Chloro-4-fur-2-ylpyrimidine 97%, 2-Chloro-4-(Furan-2-Yl)Pyrimidine

2-Chloro-4-(fur-2-yl)pyrimidine

2-Chloro-4-(fur-2-yl)pyrimidine is a reactive compound with various applications. It has been studied for its antinociceptive properties, meaning it can help reduce pain sensation. This compound has also shown potential as an electrode material in electronic devices. Additionally, 2-Chloro-4-(fur-2-yl)pyrimidine is used in the synthesis of polyketides, which are important organic compounds with diverse biological activities.

Furthermore, this compound has been found to interact with cannabinoid receptors, suggesting potential therapeutic applications in the field of medicine. It has also demonstrated collagen-stimulating properties and the ability to modulate fatty acid metabolism. These characteristics make it a valuable component in biomaterials research.

Moreover, 2-Chloro-4-(fur-2-yl)pyrimidine can form boron complex salts that exhibit cytotoxic effects on certain cancer cells. This compound has also been investigated for its potential use as

CAS 124959-28-0: 2-Chloro-4-(2-furyl)pyrimidine

2-Chloro-4-(fur-2-yl)pyrimidine

Ref: 54-OR12277

2-Chloro-4-(fur-2-yl)pyrimidine

Ref: 3D-ZEA95928

2-CHLORO-4-(2-FURYL)PYRIMIDINE

Ref: 10-F538535

Pyrimidine, 2-chloro-4-(2-furanyl)-

Ref: IN-DA000MX8