934175-49-2

Basic information

• Product Name: 2-(1H-pyrazol-1-yl)acetohydrazide(SALTDATA: FREE)
• Synonyms: 2-(1H-pyrazol-1-yl)acetohydrazide(SALTDATA: FREE);2-(1H-Pyrazol-1-yl)acetohydrazide;2-(1-pyrazolyl)acetohydrazide;2-pyrazol-1-ylacetohydrazide;2-pyrazol-1-ylethanehydrazide
• CAS NO: 934175-49-2
• Molecular Formula: C5H8N4O
• Molecular Weight: 140.14322
• Mol File: 934175-49-2.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-(1H-pyrazol-1-yl)acetohydrazide(SALTDATA: FREE)(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(1H-pyrazol-1-yl)acetohydrazide(SALTDATA: FREE)(934175-49-2)
• EPA Substance Registry System: 2-(1H-pyrazol-1-yl)acetohydrazide(SALTDATA: FREE)(934175-49-2)

Safety Data

• Hazardous Substances Data: 934175-49-2(Hazardous Substances Data)

Usage

General Description

2-(1H-pyrazol-1-yl)acetohydrazide, also known as SALTDATA: FREE, is a chemical compound with the molecular formula C5H8N4O. It is a hydrazide derivative with a pyrazole ring, and is commonly used in organic synthesis and pharmaceutical research. 2-(1H-pyrazol-1-yl)acetohydrazide(SALTDATA: FREE) has potential activity as an anti-inflammatory and analgesic agent, as well as antipyretic properties. It is also being investigated for its potential use in the treatment of various diseases, such as cancer and neurodegenerative disorders. Additionally, SALTDATA: FREE has been studied for its antimicrobial and antiviral activities, showing promising results in inhibiting the growth of certain pathogens. Overall, this compound has a wide range of potential applications and is a subject of ongoing research in the fields of medicine and drug development.

Upstream product

• 10199-61-8 pyrazol-1-yl acetic acid ethyl ester 

Relevant articles and documents

Antimicrobial Evaluation, Synthesis, and Characterization of Some 1-(5-((1H-Pyrazol-1-yl)methyl)-2-aryl-1,3,4-oxadiazol-3(2H)-yl)ethanone Derivatives

Ethyl 2-(1H-pyrazol-1-yl)acetate (1) was synthesized by the reaction of ethyl chloro acetate with 1H-pyrazole. Compound (1) was refluxed with hydrazine hydrate to get 2-(1H-pyrazol-1-yl) acetohydrazide (2). N'-arylidine-2-(1H-pyrazol-1-yl)acetohydrazide d

Synthesis of N- and C-azolyl-substituted pyrazolo[1,5-a]pyrimidines by recyclization of pyrimidinium salts

We studied the reaction of 2-(ethoxycarbonyl)methyl-1,4,6-trimethylpyrimidinium iodide with hydrazides of N-azolyl- and C-pyrazolyl-substituted carboxylic acids, which were synthesized by reacting the respective esters with hydrazine hydrate. This reaction was shown to result in recyclization and formation of ethyl 2-(pyrazolylalkyl)- and 2-(azolylalkyl)-5,7-dimethylpyrazolo[1,5-a]pyrimidine- 3-carboxylates. Besides pyrazolopyrimidines, the separation of reaction mixture provided in some cases also another recyclization product, 2-hydroxy-5,7-dimethylpyrazolo[1,5-a]pyrimidine.