26033-27-2 Usage
Uses
Used in Organic Synthesis:
3-(2-Thienyl)-1H-pyrazole-4-carbaldehyde is used as a key intermediate in organic synthesis for the preparation of various complex organic molecules. Its unique structure allows for versatile chemical reactions, making it a valuable component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 3-(2-Thienyl)-1H-pyrazole-4-carbaldehyde is used as a building block for the development of novel drug candidates. Its heterocyclic nature and functional groups enable the design of molecules with potential therapeutic properties, such as antimicrobial, antiviral, or anticancer activities. Further research is required to explore its pharmacological potential and optimize its properties for specific medical applications.
Used in Materials Science:
3-(2-Thienyl)-1H-pyrazole-4-carbaldehyde may also find applications in materials science, particularly in the development of new materials with unique electronic, optical, or magnetic properties. Its heterocyclic structure and functional groups can be utilized to create novel polymers, coordination compounds, or other advanced materials with potential applications in electronics, sensors, or energy storage devices.
Check Digit Verification of cas no
The CAS Registry Mumber 26033-27-2 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 7 respectively.
Calculate Digit Verification of CAS Registry Number 26033-27:
(7*2)+(6*6)+(5*0)+(4*3)+(3*3)+(2*2)+(1*7)=82
82 % 10 = 2
So 26033-27-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H6N2OS/c11-5-6-4-9-10-8(6)7-2-1-3-12-7/h1-5H,(H,9,10)
26033-27-2Relevant 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
A new synthethic approach to indazole synthesis
Baraldi, Pier Giovanni,Cacciari, Barbara,Spalluto, Giampiero,Romagnoli, Romeo,Braccioli, Giovanni,Zaid, Abdel Naser,De Pineda Las Infantas, Maria J.
, p. 1140 - 1142 (2007/10/03)
Stobbe condensation of 3-alkyl- or aryl-4-formylpyrazoles 3a-f with diethyl succinate in the presence of potassium f-butoxide, followed by intramolecular ring closure (Ac2O-NaOAc), afforded the corresponding indazole derivatives 5a-f in 65-85% overall yield. These compounds are good starting materials for transformation to biologically active molecules, such as new pyrazole analogs of the left-hand segment of the potent natural antineoplastic agent CC-1065.
