1-(6-Methylpyrimidin-4-yl)ethanone, with the CAS number 67073-96-5, is an organic compound characterized by its pyrimidine ring structure, which is a six-membered aromatic heterocycle containing nitrogen atoms. This compound features a ketone functional group (ethanone) attached to the pyrimidine ring, specifically at the 4-position, with a methyl group at the 6-position. The presence of the methyl group contributes to its hydrophobic character, influencing its solubility and reactivity. Typically, compounds like this may exhibit biological activity, making them of interest in medicinal chemistry and drug development. The molecular structure allows for potential interactions with biological targets, and its properties can be influenced by factors such as pH and solvent polarity. Additionally, the compound may participate in various chemical reactions, including nucleophilic substitutions and condensation reactions, due to the reactivity of the carbonyl group. Overall, 1-(6-methylpyrimidin-4-yl)ethanone is a versatile compound with applications in research and industry.

1-(6-methylpyrimidin-4-yl)ethanone

67073-96-5: 1-(6-Methylpyrimidin-4-yl)ethanone, with the CAS number 67073-96-5, is an organic compound characterized by its pyrimidine ring structure, which is a six-membered aromatic heterocycle containing nitrogen atoms. This compound features a ketone functional group (ethanone) attached to the pyrimidine ring, specifically at the 4-position, with a methyl group at the 6-position. The presence of the methyl group contributes to its hydrophobic character, influencing its solubility and reactivity. Typically, compounds like this may exhibit biological activity, making them of interest in medicinal chemistry and drug development. The molecular structure allows for potential interactions with biological targets, and its properties can be influenced by factors such as pH and solvent polarity. Additionally, the compound may participate in various chemical reactions, including nucleophilic substitutions and condensation reactions, due to the reactivity of the carbonyl group. Overall, 1-(6-methylpyrimidin-4-yl)ethanone is a versatile compound with applications in research and industry.

CAS 67073-96-5

1-(6-methylpyrimidin-4-yl)ethanone

Ethanone,1-(6-methyl-4-pyrimidinyl)-

Ref: IN-DA006M6B

1-(6-Methylpyrimidin-4-yl)ethan-1-one

Ref: 54-OR94003

1-(6-Methylpyrimidin-4-yl)ethanone

Ref: 10-F091667