CAS 4786-51-0

4-aminopyrimidine-5-carboxamide

Description:

4-Aminopyrimidine-5-carboxamide, with the CAS number 4786-51-0, is an organic compound characterized by its pyrimidine ring structure, which features an amino group (-NH2) at the 4-position and a carboxamide group (-C(=O)NH2) at the 5-position. This compound is typically a white to off-white crystalline solid, soluble in polar solvents such as water and alcohols, owing to the presence of the carboxamide functional group that can engage in hydrogen bonding. It exhibits basic properties due to the amino group, which can accept protons. The compound is of interest in various fields, including medicinal chemistry, where it may serve as a building block for pharmaceuticals or as a potential therapeutic agent. Its reactivity can be influenced by the functional groups present, allowing for various chemical transformations. Additionally, 4-aminopyrimidine-5-carboxamide may exhibit biological activity, making it a subject of research in drug development and related studies.

Formula: C₅H₆N₄O

InChI: InChI=1/C5H6N4O/c6-4-3(5(7)10)1-8-2-9-4/h1-2H,(H2,7,10)(H2,6,8,9)

SMILES: c1c(c(=N)[nH]cn1)C(=N)O

Synonyms:

• 5-Pyrimidinecarboxamide, 4-Amino-

5-Pyrimidinecarboxamide, 4-amino- (6CI,7CI,8CI,9CI)

CAS: 4786-51-0

Formula: C₅H₆N₄O

Purity: 97%

Color and Shape: Solid

Molecular weight: 138.1273

Ref: IN-DA00DC5K

4-amino-5-pyrimidinecarboxamide

CAS: 4786-51-0

Formula: C₅H₆N₄O

Purity: 97%

Color and Shape: Solid

Molecular weight: 138.13

Ref: 10-F311292

4-aminopyrimidine-5-carboxamide

CAS: 4786-51-0

4-Aminopyrimidine-5-carboxamide is an amide that is synthesized from the reaction of eosinophil and amine. This compound inhibits transcription in a dose-dependent manner, with a high potency for iminium and amines, but not primary amines. 4-Aminopyrimidine-5-carboxamide is orally bioavailable and has shown to be effective in animal models. The compound has been optimized for oral administration and has shown to produce good yields. 4-Aminopyrimidine-5-carboxamide also possesses transcription factor inhibitory activity against interleukin, which may provide therapeutic benefit for inflammatory disorders.

Formula: C₅H₆N₄O

Purity: Min. 95%

Molecular weight: 138.13 g/mol

Ref: 3D-EAA78651