4-Chloro-6-methyl-2-phenylpyrimidine is an organic compound characterized by its pyrimidine ring structure, which is a six-membered aromatic ring containing two nitrogen atoms at positions 1 and 3. The presence of a chloro group at position 4 and a methyl group at position 6, along with a phenyl group at position 2, contributes to its unique chemical properties. This compound is typically a solid at room temperature and is known for its potential applications in pharmaceuticals and agrochemicals due to its biological activity. It may exhibit various functional properties, including antimicrobial and anti-inflammatory effects, making it of interest in medicinal chemistry. The molecular structure allows for interactions with biological targets, which can be explored in drug development. Additionally, its solubility and reactivity can vary depending on the solvent and conditions, influencing its use in synthetic pathways. Safety data should be consulted for handling, as halogenated compounds can pose environmental and health risks.

4-chloro-6-methyl-2-phenylpyrimidine

29509-92-0: Pyrimidine, 4-Chloro-6-Methyl-2-Phenyl-, 4-CHLORO-6-METHYL-2-PHENYLPYRIMIDINE

4-Chloro-6-methyl-2-phenylpyrimidine (4CMP) is a synthetic analogue of phenylpyruvate that exhibits electrophilic properties and has been shown to be a potent inhibitor of glutathione synthesis. 4CMP is known to induce apoptosis in cells and is also capable of inducing the transcriptional response associated with oxidative stress. The transcriptome data show that 4CMP induces expression of genes associated with lipid biosynthesis and fatty acid oxidation, as well as certain oxylipins and their synthesizing enzymes. These findings suggest that 4CMP may have an inhibitory effect on the synthesis of fatty acids, which are important for cellular metabolism and membrane integrity. The transcriptional response induced by 4CMP indicates that it has the ability to amplify the effects of other oxidative stresses by inducing the production of specific oxylipins such as 12(S)-HETE. This compound can also be used in abiotic processes

CAS 29509-92-0: 4-chloro-6-methyl-2-phenylpyrimidine

4-Chloro-6-methyl-2-phenylpyrimidine

Ref: 3D-FC118971

Pyrimidine, 4-chloro-6-methyl-2-phenyl-

Ref: IN-DA002YLP

4-Chloro-6-methyl-2-phenyl-pyrimidine

Ref: 10-F058300