CAS 246048-63-5

1,2,5-Oxadiazole-3-carboximidicacid, 4-amino-, methyl ester

Description:

1,2,5-Oxadiazole-3-carboximidic acid, 4-amino-, methyl ester is a chemical compound characterized by its oxadiazole ring, which is a five-membered heterocyclic structure containing two nitrogen atoms and three carbon atoms. This compound features a carboximidic acid functional group, which contributes to its potential as a bioactive molecule. The presence of the methyl ester group enhances its solubility and reactivity, making it suitable for various chemical reactions and applications. The 4-amino substitution indicates the presence of an amino group at the fourth position of the oxadiazole ring, which can participate in hydrogen bonding and influence the compound's biological activity. This compound may exhibit properties such as antimicrobial or anti-inflammatory activities, making it of interest in pharmaceutical research. Its unique structure allows for potential modifications that could lead to the development of new therapeutic agents. As with many heterocycles, the stability and reactivity of this compound can be influenced by environmental factors such as pH and temperature.

Formula: C₄H₆N₄O₂

Synonyms:

• 4-Amino-1,2,5-oxadiazole-3-carboximidicacid methyl ester

Methyl 4-amino-1,2,5-oxadiazole-3-carboximidate

CAS: 246048-63-5

Methyl 4-amino-1,2,5-oxadiazole-3-carboximidate is a small molecule that can be synthesized from amines and triazoles. It undergoes an intramolecular cyclization to form a hydrazine and an acylhydrazine. This reaction is facilitated by the presence of nitrogen containing groups such as amidines or amidrazones. The yields of these reactions are high, making this compound a good starting material for the synthesis of aromatic amines.

Formula: C₄H₆N₄O₂

Purity: Min. 95%

Molecular weight: 142.12 g/mol

Ref: 3D-WJA04863