32332-98-2 Usage
Uses
Used in Pharmaceutical Industry:
3-Fur-2-yl-1H-pyrazole is utilized as a pharmaceutical agent for its anti-inflammatory properties, offering potential therapeutic benefits in treating inflammation-related conditions. Its anti-cancer activity makes it a promising candidate for the development of novel cancer treatments, targeting various types of cancer cells and potentially synergizing with existing chemotherapeutic drugs to enhance their efficacy.
Used in Agrochemical Industry:
In the agrochemical sector, 3-Fur-2-yl-1H-pyrazole is employed as a bioactive compound with anti-viral properties, which can be incorporated into formulations for protecting crops from viral infections, thereby improving agricultural productivity and crop health.
Used in Chemical Synthesis:
3-Fur-2-yl-1H-pyrazole serves as a key building block in the synthesis of a variety of biologically active compounds. Its unique structure allows for the creation of new molecules with potential applications in medicine, agriculture, and other fields, contributing to the advancement of chemical research and the development of innovative products.
Check Digit Verification of cas no
The CAS Registry Mumber 32332-98-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,3,3 and 2 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 32332-98:
(7*3)+(6*2)+(5*3)+(4*3)+(3*2)+(2*9)+(1*8)=92
92 % 10 = 2
So 32332-98-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H6N2O/c1-2-7(10-5-1)6-3-4-8-9-6/h1-5H,(H,8,9)
32332-98-2Relevant academic research and scientific papers
Saito, Katsuhiro,Sato, Tatsuji,Ishihara, Hiraku,Takahashi, Kensuke
, p. 1925 - 1929 (1989)
Reactions of the sodium salts of tosylhydrazones of several heteroaromatic aldehydes with an equimolar amount of acrylonitrile afforded the corresponding cyclopropane derivatives as the major products accompanied by small amounts of pyrazole derivatives.On the other hand, reactions using ten-molar equivalents of acrylonitrile gave pyrazole derivatives as major products.
Syntheses, structures and electrochemistry of [CuL1(LR)]BF4 [L1 = 3-{2,5-dimethoxyphenyl-1-(2-pyridyl)pyrazole; LR = tris(3-arylpyrazolyl)hydroborate] and [CuL12][BF4]
Halcrow, Malcolm A.,McInnes, Eric J. L.,Mabbs, Frank E.,Scowen, Ian J.,McPartlin, Mary,Powell, Harold R.,Davies, John E.
, p. 4025 - 4035 (2007/10/03)
Reaction of potassium 3(5)-(2,5-dimethoxyphenyl)pyrazolate with 2-bromopyridine in diglyme (2,5,8-trioxanonane) at 130°C for 3 d afforded 3-(2,5-dimethoxyphenyl)-1-(2-pyridyl)pyrazole (L1) in 69% yield after an aqueous quench and recrystallisat
