53666-79-8

Usage

Uses

Used in Pharmaceutical and Agrochemical Industries:
3-amino-1H-pyrazol-5-ol is utilized as a building block in the synthesis of pharmaceuticals and agrochemicals, contributing to the development of new drugs and pesticides due to its unique chemical structure and properties.
Used in Chemical Research:
3-amino-1H-pyrazol-5-ol serves as a reagent in chemical research, aiding in the exploration of new chemical reactions and the synthesis of novel compounds.
Used in Corrosion Inhibition:
3-amino-1H-pyrazol-5-ol has been investigated for its potential as a corrosion inhibitor, offering a possible solution for protecting materials from degradation in various industrial applications.
Used in Therapeutic Applications:
3-amino-1H-pyrazol-5-ol is studied for its anti-inflammatory and anti-cancer activities, indicating its potential use in the development of treatments for inflammatory diseases and cancer therapies.

InChI:InChI=1/C3H5N3O/c4-2-1-3(7)6-5-2/h1H,(H4,4,5,6,7)

Downstream Products

• 119769-05-0 3-amino-5-hydroxy-1H-pyrazole-1-carboxamide 
• 28491-58-9 3,6-Dihydroxy-4-methyl-1-pyrazolo<3.4-b>pyridin 
• 1219743-00-6 5-(cyclopropylmethoxy)-1H-pyrazol-3-amine 
• 1150263-09-4 5-[(3,5-dimethoxyphenyl)methoxy]-2H-pyrazol-3-amine hydrochloride 
• 121507-34-4 5-propan-2-yloxy-1H-pyrazol-3-amine 
• 1000896-51-4 5-[(3-fluorophenyl)methoxy]-1H-pyrazol-3-amine 
• 1150263-09-4 5-[(3,5-dimethoxyphenyl)methoxy]-1H-pyrazol-3-amine.HCl 
• 1160822-76-3 2-(3-hydroxy-1H-pyrazol-5-yl)isoindoline-1,3-dione 
• 1160822-76-3 2-(5-hydroxy-1H-pyrazol-3-yl)isoindoline-1,3-dione 
• 120292-05-9 5-(2-methoxyethoxy)-1H-pyrazol-3-amine 
• 1233690-31-7 C₁₈H₁₂N₄O₆ 
• 1233690-21-5 C₂₄H₂₅N₃O₄ 
• 1233690-25-9 C₂₆H₂₉N₃O₄ 
• 1233690-18-0 C₁₈H₁₃N₃O₃ 

Relevant academic research and scientific papers

Method of treating a patient having precancerous lesions with phenyl cycloamino pyrimidinone derivatives

Derivatives of Phenyl Cycloamino Pyrimidinone are useful for the treatment of patients having precancerous lesions. These compounds are also useful to inhibit growth of neoplastic cells.

PYRIDOPYRIMIDINONE ANTIANGINAL AGENTS

Compounds of the formula and pharmaceutically acceptable salts thereof, wherein R 1 is H, C 1 -C 4 alkyl CN or CONR 4 R 5 ; R 2 is C 2 -C 4 alkyl; R 3 is SO 2 NR 6 R 7, NO 2, NH 2, NHCOR 8 NHSO 2 R 8 or N(SO 2 R 8) 2 ; R 4 and R 5 are each independently selected from H and C 1 -C 4 alkyl; R 6 and R 7 are each independently selected from H and C 1 -C 4 alkyl optionally substituted with CO 2 R 9, OH, pyridyl 5-isoxazolin-3-onyl, morpholino or 1-imidazolidin-2-onyl; or together with the nitrogen atom to which they are attached form a pyrrolidino, piperidino, morpholino, 1-pyrazolyl or 4-(NR 10)-1-piperazinyl group wherein any of said groups may optionally be substituted with one or two substituents selected from C 1 -C 4 alkyl, CO 2 R 9, NH 2 and OH; R 8 is C 1 -C 4 alkyl or pyridyl; R 9 is H or C 1 -C 4 alkyl; and R 10 is H, C 1 -C 4 alkyl or (hydroxy) C 2 -C 3 alkyl; are selected cGMP PDE inhibitors useful in the treatment of, inter alia, cardiovascular disorders such as angina, hypertension, heart failure and atherosclerosis

Aminopyrazoles

The present invention relates to compounds, compositions and methods for inhibiting nonenzymatic cross-linking (protein aging). Accordingly, a composition is disclosed which comprises aminopyrazoles capable of inhibiting the formation of advanced glycosylation endproducts of target proteins by reacting with the carbonyl moiety of an early glycosylation product of such target proteins formed by their initial glycosylation. The method comprises contacting the target protein with the composition. Both industrial and therapeutic applications for the invention are envisioned, as food spoilage and animal protein aging can be treated.