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CAS 66373-25-9

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5-Acetyl-2-amino-4-methylpyrimidine

Description:
5-Acetyl-2-amino-4-methylpyrimidine is an organic compound characterized by its pyrimidine ring structure, which is a six-membered aromatic ring containing two nitrogen atoms at the 1 and 3 positions. This compound features an acetyl group at the 5-position and an amino group at the 2-position, along with a methyl group at the 4-position of the pyrimidine ring. It is typically a crystalline solid and is soluble in polar solvents due to the presence of the amino group, which can engage in hydrogen bonding. The compound is of interest in various fields, including medicinal chemistry, due to its potential biological activities and applications in the synthesis of pharmaceuticals. Its molecular structure allows for various chemical reactions, making it a versatile intermediate in organic synthesis. Additionally, the presence of functional groups such as the acetyl and amino groups can influence its reactivity and interactions with other molecules.
Formula:C7H9N3O
InChI:InChI=1/C7H9N3O/c1-4-6(5(2)11)3-9-7(8)10-4/h3H,1-2H3,(H2,8,9,10)
SMILES:Cc1c(c[nH]c(=N)n1)C(=O)C
Synonyms:
  • 1-(2-Amino-4-methyl-5-pyrimidinyl)ethanone
  • 1-(2-Amino-4-Methylpyrimidin-5-Yl)Ethan-1-One
  • 1-(2-Amino-4-methylpyrimidin-5-yl)ethanone
  • 2-Amino-4-methyl-5-pyrimidyl methyl ketone
  • Ethanone, 1-(2-Amino-4-Methyl-5-Pyrimidinyl)-
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