3-Amino-5-methyl-1H-pyrazole-4-carbonitrile is an organic compound characterized by its pyrazole ring structure, which is a five-membered ring containing two nitrogen atoms. This compound features an amino group (-NH2) and a cyano group (-C≡N) attached to the pyrazole ring, contributing to its reactivity and potential applications in various fields, including pharmaceuticals and agrochemicals. The presence of the methyl group at the 5-position enhances its lipophilicity, which can influence its biological activity. The compound is typically a solid at room temperature and may exhibit moderate solubility in polar solvents. Its chemical properties are influenced by the functional groups present, making it a candidate for further chemical modifications. Additionally, 3-amino-5-methyl-1H-pyrazole-4-carbonitrile may exhibit biological activities, such as antimicrobial or anti-inflammatory effects, which are of interest in medicinal chemistry. Safety data should be consulted for handling and usage, as with any chemical substance.

3-amino-5-methyl-1H-pyrazole-4-carbonitrile

5453-07-6: 1H-pyrazole-4-carbonitrile, 5-amino-3-methyl-, 5-Amino-3-methyl-1H-pyrazole-4-carbonitrile

5-Amino-3-methyl-1H-pyrazole-4-carbonitrile is a modified purine that inhibits purine synthesis. It has been shown to be effective in treating tropical diseases, such as malaria and dengue fever, which are caused by protozoans. The natural product has been synthesized via solid phase methods and yields of the product were optimized for medicinal use. 5-Amino-3-methyl-1H-pyrazole-4-carbonitrile is also a pyrimidine nucleoside analogue that has been used in the treatment of HIV patients.

CAS 5453-07-6: 3-amino-5-methyl-1H-pyrazole-4-carbonitrile

3-amino-5-methyl-1H-pyrazole-4-carbonitrile

Ref: IN-DA00DACP

5-Amino-3-methyl-1H-pyrazole-4-carbonitrile

Ref: 3D-FA134677

5-Amino-3-methyl-1H-pyrazole-4-carbonitrile

Ref: 10-F236934

3-Amino-4-cyano-5-methylpyrazole

Ref: 54-OR300740