CAS 20737-41-1

4-Aminopyrimidine-5-carboxylic acid

Description:

4-Aminopyrimidine-5-carboxylic acid, with the CAS number 20737-41-1, is an organic compound characterized by its pyrimidine ring structure, which features an amino group (-NH2) at the 4-position and a carboxylic acid group (-COOH) at the 5-position. This compound is typically a white to off-white crystalline solid and is soluble in water and polar organic solvents, reflecting its polar functional groups. It exhibits properties typical of both amines and carboxylic acids, such as the ability to participate in hydrogen bonding, which can influence its reactivity and interactions in biological systems. 4-Aminopyrimidine-5-carboxylic acid is of interest in medicinal chemistry and biochemistry, as it may serve as a building block for the synthesis of various pharmaceuticals or as a potential therapeutic agent. Its structural features allow it to interact with biological targets, making it a subject of research in drug development and related fields.

Formula: C₅H₅N₃O₂

InChI: InChI=1/C5H5N3O2/c6-4-3(5(9)10)1-7-2-8-4/h1-2H,(H,9,10)(H2,6,7,8)

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

Synonyms:

• Akos Bbs-00002112
• 4-Amino-5-Pyrimidinecarboxylic Acid
• Buttpark 33\08-70
• Rarechem Al Bo 1509
• 5-Pyrimidinecarboxylic acid, 4-amino- (6CI,7CI,8CI,9CI)

5-Pyrimidinecarboxylic acid, 4-amino-

CAS: 20737-41-1

Formula: C₅H₅N₃O₂

Purity: 96%

Color and Shape: Solid

Molecular weight: 139.1121

Ref: IN-DA002J0J

4-Aminopyrimidine-5-carboxylic acid

CAS: 20737-41-1

4-Aminopyrimidine-5-carboxylic acid

Formula: C₅H₅N₃O₂

Purity: 96%

Color and Shape: faint yellow solid

Molecular weight: 139.11g/mol

Ref: 54-OR13043

4-Aminopyrimidine-5-carboxylic acid

CAS: 20737-41-1

Formula: C₅H₅N₃O₂

Purity: 95%

Color and Shape: Solid

Molecular weight: 139.114

Ref: 10-F017338

4-Aminopyrimidine-5-carboxylic acid

CAS: 20737-41-1

4-Aminopyrimidine-5-carboxylic acid is an aminopyrimidone that has been synthesized to be used as a new class of antihypertensive agents. It has dose-dependent blood pressure lowering effects, which are likely due to its ability to block angiotensin receptors. 4-Aminopyrimidine-5-carboxylic acid also has antibacterial and antifungal properties. This compound is metabolized in vivo into the pharmacologically active amine 6-aminonicotinamide and excreted in the urine. In vitro studies have shown that 4-aminopyrimidine-5 carboxylic acid inhibits the growth of bacteria by binding to DNA gyrase and topoisomerase IV enzymes required for cell division.

Formula: C₅H₅N₃O₂

Purity: Min. 95%

Molecular weight: 139.11 g/mol

Ref: 3D-NA57368