CAS 14493-37-9

1-aminopyrimidine-2,4(1H,3H)-dione

Description:

1-Aminopyrimidine-2,4(1H,3H)-dione, also known as 2,4-dioxo-1-pyrimidinamine, is an organic compound characterized by its pyrimidine ring structure, which features an amino group and two carbonyl groups. This compound typically appears as a crystalline solid and is soluble in polar solvents, reflecting its ability to engage in hydrogen bonding due to the presence of the amino and carbonyl functional groups. It exhibits basic properties due to the amino group, allowing it to participate in various chemical reactions, including nucleophilic substitutions and condensation reactions. The presence of the dione functionality contributes to its potential reactivity, making it a valuable intermediate in organic synthesis and medicinal chemistry. Additionally, 1-aminopyrimidine-2,4(1H,3H)-dione may exhibit biological activity, which can be explored for pharmaceutical applications. Its structural features and reactivity make it a compound of interest in the development of new drugs and agrochemicals.

Formula: C₄H₅N₃O₂

InChI: InChI=1/C4H5N3O2/c5-7-2-1-3(8)6-4(7)9/h1-2H,5H2,(H,6,8,9)

SMILES: c1cn(c(=O)nc1O)N

Synonyms:

• 2,4(1H,3H)-Pyrimidinedione, amino-
• Amino-2,4(1H,3H)-pyrimidinedione

1-Amino-1,2,3,4-tetrahydropyrimidine-2,4-dione

CAS: 14493-37-9

1-Amino-1,2,3,4-tetrahydropyrimidine-2,4-dione is an alkynyl amine that is used in the agricultural industry as a binding agent for acid. It has been shown to bind to cyanoalkyl, haloalkyl and aminouracil groups. The compound also has a variety of other uses in the pharmaceutical industry including use as a nerve toxin. 1-Amino-1,2,3,4-tetrahydropyrimidine-2,4-dione is also used as a spectrum diluent and can be used in refluxing reactions with nitro compounds.

Formula: C₄H₅N₃O₂

Purity: Min. 95%

Molecular weight: 127.1 g/mol

Ref: 3D-PAA49337