CAS 54568-11-5
:4,5,6-trimethylpyrimidin-2-amine
Description:
4,5,6-Trimethylpyrimidin-2-amine is an organic compound characterized by its pyrimidine ring structure, which is a six-membered aromatic heterocycle containing nitrogen atoms. Specifically, this compound features three methyl groups attached to the pyrimidine ring at the 4, 5, and 6 positions, and an amino group at the 2 position. This configuration contributes to its unique chemical properties, including its potential solubility in polar solvents and its reactivity due to the presence of the amino group, which can participate in various chemical reactions, such as nucleophilic substitutions. The compound may exhibit biological activity, making it of interest in pharmaceutical research. Its molecular structure allows for interactions with biological systems, potentially influencing enzyme activity or acting as a precursor in the synthesis of other compounds. Additionally, the presence of multiple methyl groups can affect the compound's steric and electronic properties, influencing its stability and reactivity. Overall, 4,5,6-trimethylpyrimidin-2-amine is a versatile compound with applications in organic synthesis and medicinal chemistry.
Formula:C7H11N3
InChI:InChI=1/C7H11N3/c1-4-5(2)9-7(8)10-6(4)3/h1-3H3,(H2,8,9,10)
SMILES:Cc1c(C)[nH]c(=N)nc1C
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Found 1 products.
4,5,6-Trimethylpyrimidin-2-amine
CAS:<p>4,5,6-Trimethylpyrimidin-2-amine is a human immunodeficiency virus (HIV) type 1 inhibitor that is currently in the early stages of development. It has shown antiviral activity against HIV type 1 strains and cytotoxicity against HIV-infected cells. In vitro studies have shown that 4,5,6-trimethylpyrimidin-2-amine inhibits the HIV transcriptional elongation factor TFIIS by binding to the enzyme. This inhibition leads to a decrease in viral RNA synthesis and consequently a decrease in virus production.</p>Formula:C7H11N3Purity:Min. 95%Molecular weight:137.18 g/mol
