CAS 40424-48-4

4(1H)-Pyrimidinethione, 5-amino-6-methoxy-

Description:

4(1H)-Pyrimidinethione, 5-amino-6-methoxy- is an organic compound characterized by its pyrimidine ring structure, which is a six-membered aromatic heterocycle containing two nitrogen atoms at positions 1 and 3. This compound features a thione functional group, indicating the presence of a sulfur atom double-bonded to a carbon atom, which contributes to its reactivity and potential biological activity. The amino group at position 5 and the methoxy group at position 6 enhance its solubility and may influence its interaction with biological targets. This compound is of interest in medicinal chemistry due to its potential applications in pharmaceuticals, particularly in the development of antimicrobial or anticancer agents. Its properties, such as melting point, solubility, and spectral characteristics, are influenced by the presence of these functional groups. As with many heterocyclic compounds, it may exhibit unique electronic properties and reactivity patterns, making it a subject of study in various chemical and biological contexts.

Formula: C₅H₇N₃OS

5-Amino-6-methoxy-3,4-dihydropyrimidine-4-thione

CAS: 40424-48-4

5-Amino-6-methoxy-3,4-dihydropyrimidine-4-thione is an organic solvent that belongs to the heterocycles group. It is a pyrimidine derivative of acrylonitrile with a carbanion. The reaction products are dicarbonyl compounds and hydroxylamine. 5-Amino-6-methoxy-3,4-dihydropyrimidine-4-thione reacts with chloride in the presence of sulfur to form tetracyclic products. This compound has been used for researches and as a reagent for the formation of other organic compounds.

Formula: C₅H₇N₃OS

Purity: Min. 95%

Molecular weight: 157.2 g/mol

Ref: 3D-QBA42448