Ethyl 3-aminopyrazole-4-carboxylate

CAS: 6994-25-8

Ref. 3D-IE09849

Product Information

• Name: Ethyl 3-aminopyrazole-4-carboxylate
• Synonyms: Allopurinol impurity D3-Amino-4-pyrazolecarboxylic acid ethyl ester, 1H-Pyrazole-4-carboxylic acid, 3-amino-, ethyl ester, 1H-Pyrazole-4-carboxylic acid, 5-amino-, ethyl ester, 3-Amino-4-(ethoxycarbonyl)pyrazole, 3-Amino-4-carbethoxypyrazole, 3-Amino-4-carboethoxy-2H-pyrazole, 3-Amino-4-pyrazolecarboxylic acid ethyl ester, 5-Amino-1H-pyrazole-4-carboxylic acid ethyl ester, Ethyl 3-amino-1H-pyrazole-4-carboxylate, Ethyl 3-amino-4-pyarazolecarboxylate, Ethyl 3-amino-4-pyrazolecarboxylate, Ethyl 3-aminopyrazol-4-carboxylate, Ethyl 5-Amino-1H-4-Pyrazolecarboxylate, Ethyl 5-amino-1H-pyrazole-4-carboxylate, Ethyl 5-amino-4-pyrazolecarboxylate, Ethyl 5-aminopyrazol-4-carboxylate, Ethyl-5-amino-1H-pyrazol-4-carboxylat, NSC 521580, Pyrazole-4-carboxylic acid, 3(or 5)-amino-, ethyl ester, Pyrazole-4-carboxylic acid, 3-amino-, ethyl ester

Description

Ethyl 3-aminopyrazole-4-carboxylate is an anticancer drug that inhibits the growth of cancer cells by inhibiting protein synthesis. It has been shown to inhibit the activity of dpp-iv and pde5, which are enzymes involved in cellular proliferation. Ethyl 3-aminopyrazole-4-carboxylate has also been shown to have antiinflammatory properties, which may be due to inhibition of prostaglandin synthesis.
Ethyl 3-aminopyrazole-4-carboxylate is a multinuclear compound that reacts with nitrogen atoms from the pyrazoles to form a stable molecule. Dimethylformamide is used as a solvent for this reaction. The synthesis of ethyl 3-aminopyrazole-4-carboxylate starts with acetylation, which converts the carboxylic acid group into an acetic acid group. The acetic acid group reacts with ammonia and hydrogen cyan

• Brand: Biosynth

Chemical properties

• Molecular weight: 155.16 g/mol
• Formula: C₆H₉N₃O₂
• Purity: Min. 95%
• Color/Form: Powder