123834-58-2 Usage
Chemical structure
1,4-Benzenediol, 2,3-di-1H-pyrazol-1-ylis a chemical compound with a benzene ring and two hydroxyl groups at the 1 and 4 positions, and two pyrazole rings attached at the 2 and 3 positions.
Potential biological activity
1,4-Benzenediol, 2,3-di-1H-pyrazol-1-yl- has been of interest in medicinal chemistry due to its potential as a drug candidate.
Antioxidant properties
The structure of 1,4-Benzenediol, 2,3-di-1H-pyrazol-1-ylsuggests that it may have antioxidant properties, which could be useful in the treatment of various diseases.
Anti-inflammatory properties
The compound may also possess anti-inflammatory properties, which could be beneficial in the treatment of inflammatory conditions.
Applications in medicinal chemistry
1,4-Benzenediol, 2,3-di-1H-pyrazol-1-ylis currently being studied for its potential use in the treatment of various diseases, including those related to oxidative stress and inflammation.
Applications in materials science
Due to its unique structure, 1,4-Benzenediol, 2,3-di-1H-pyrazol-1-ylmay have potential applications in materials science, such as in the development of new materials with specific properties.
Applications in organic synthesis
The compound may also be useful in organic synthesis, as a building block or intermediate for the synthesis of other complex molecules.
Ongoing research
Further studies are needed to fully understand the properties and potential applications of 1,4-Benzenediol, 2,3-di-1H-pyrazol-1-ylin various fields, including medicinal chemistry, materials science, and organic synthesis.
Check Digit Verification of cas no
The CAS Registry Mumber 123834-58-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,8,3 and 4 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 123834-58:
(8*1)+(7*2)+(6*3)+(5*8)+(4*3)+(3*4)+(2*5)+(1*8)=122
122 % 10 = 2
So 123834-58-2 is a valid CAS Registry Number.
123834-58-2Relevant academic research and scientific papers
Reaction of Pyrazole Adddition to Quinones
Ballesteros, Paloma,Claramunt, Rosa M.,Escolastico, Consuelo,Maria, M. Dolores Santa,Elguero, Jose
, p. 1873 - 1876 (2007/10/02)
The reactions of pyrazole, 4-nitropyrazole, 3,5-dimethylpyrazole, and 4-chloro-3,5-dimethylpyrazole with 1,4-benzoquinone in dioxane have been analyzed.Mono- and 2,3-bis-adducts were obtained and only in the case of pyrazole was a 2,5-bis(pyrazol-1-yl)-1,
Photoinduced intramolecular proton transfer as the mechanism of ultraviolet stabilizers: A reappraisal
Catalán, Javier,Fabero, Fernando,Soledad Guijarro,Claramunt, Rosa M.,Dolores Santa María,De la Concepción Foces-Foces,Cano, Felix Hernández,Elguero, José,Sastre, Roberto
, p. 747 - 759 (2007/10/02)
Evidence based on theoretical calculations and photophysical experiments is presented to show that, contrary to general belief, the photostability of 2-(2′-hydroxy-5′-methylphenyl)benzotriazole (Tinuvin P) cannot be explained as being due to an excited-state intramolecular proton transfer (ESIPT) through the intramolecular hydrogen bond (IMHB). Support for this conclusion comes from a related study on several members of a new family of photostable compounds, namely the 1-(2′-hydroxyphenyl)pyrazoles, which were obtained by the reaction of pyrazole and of 3,5-dimethylpyrazole with benzoquinone. The structures of these pyrazole derivatives, namely 2,3-bis(3′,5′-dimethylpyrazol-1′-y1)-, 2,3-bis(pyrazol-1′-y1)-, 2-(pyrazol-1′-y1)-, and 2,5-bis(pyrazol-1′-y1)-1,4-dihydroxybenzene (1, 2, 3, and 4, respectively) were established by spectroscopic techniques and X-ray crystallography. Both derivatives 3 and 4 possess a strong intramolecular hydrogen bond and are reasonably photostable; derivatives 1 and 2 appear, however, to possess only a weak intramolecular hydrogen bond. 1 and 3 pack in helical systems, 4 does it with intercrossing stacking, and 2-H2O has a three-dimensional network involving water molecules.
