26033-25-0 Usage
Uses
Used in Organic Synthesis:
3-(3-NITROPHENYL)-1H-PYRAZOLE-4-CARBALDEHYDE is used as a building block for the preparation of various biologically active molecules, playing a crucial role in the creation of new organic compounds with potential applications in medicine and other industries.
Used in Pharmaceutical Research:
In Pharmaceutical Research, 3-(3-NITROPHENYL)-1H-PYRAZOLE-4-CARBALDEHYDE is utilized as a key component in the synthesis of drug candidates, contributing to the discovery and development of novel therapeutic agents.
Used as a Reagent in Chemical Reactions:
3-(3-NITROPHENYL)-1H-PYRAZOLE-4-CARBALDEHYDE serves as a reagent in various chemical reactions, facilitating the synthesis of complex molecules and aiding in the advancement of chemical processes.
Used as a Fluorescent Substance in Analytical Chemistry:
In Analytical Chemistry, 3-(3-NITROPHENYL)-1H-PYRAZOLE-4-CARBALDEHYDE is employed as a fluorescent substance, enabling the detection and analysis of specific compounds, thus enhancing the capabilities of analytical techniques.
Overall, 3-(3-NITROPHENYL)-1H-PYRAZOLE-4-CARBALDEHYDE's diverse applications across different industries highlight its significance in scientific research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 26033-25-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,0,3 and 3 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 26033-25:
(7*2)+(6*6)+(5*0)+(4*3)+(3*3)+(2*2)+(1*5)=80
80 % 10 = 0
So 26033-25-0 is a valid CAS Registry Number.
26033-25-0Relevant academic research and scientific papers
Synthesis of 3-substituted arylpyrazole-4-carboxylic acids
Lebedev,Lebedeva,Sheludyakov,Kovaleva,Ustinova,Kozhevnikov
, p. 782 - 789 (2007/10/03)
A method was suggested for preparing previously unknown 3-aryl-substituted pyrazole-4-carboxylic acids, involving Vilsmeier formylation of semicarbazones of 26 available mono- and disubstituted acetophenones and 2-acetylthiophene followed by oxidation of
