CAS 2417-17-6
:4(3H)-Pyrimidinone, 2-amino-3-methyl-
Description:
4(3H)-Pyrimidinone, 2-amino-3-methyl- 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. This compound features a keto group at the 4-position and an amino group at the 2-position, along with a methyl group at the 3-position. Its molecular formula typically reflects the presence of carbon, hydrogen, nitrogen, and oxygen atoms, contributing to its unique chemical properties. The compound is known for its potential biological activity, often studied in the context of pharmaceuticals and biochemistry. It may exhibit properties such as solubility in polar solvents and the ability to participate in hydrogen bonding due to the presence of the amino and keto functional groups. Additionally, its structure allows for various chemical reactions, including substitution and condensation, making it a valuable intermediate in organic synthesis. Overall, 4(3H)-Pyrimidinone, 2-amino-3-methyl- is significant in both research and application within medicinal chemistry.
Formula:C5H7N3O
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Found 1 products.
2-Amino-3-methyl-3,4-dihydropyrimidin-4-one
CAS:<p>2-Amino-3-methyl-3,4-dihydropyrimidin-4-one is a compound that belongs to the group of imines. It can exist as two isomers: an enamine and a ketimine. The enamine of 2-amino-3,4-dihydropyrimidin-4-one has been found to be a transition state analogue for ammonolysis reactions. The ketimine form of this compound has been shown to have tautomeric properties that are analogous to those of acetaldehyde. Chemists use spectroscopy to study the magnetic properties, dichroism, and spectra of the compound in order to learn more about its structure and reactivity.</p>Formula:C5H7N3OPurity:Min. 95%Molecular weight:125.13 g/mol
