876728-40-4 Usage
Description
5-(2-FURYL)-1-METHYL-1H-PYRAZOLE-3-CARBALDEHYDE is a chemical compound that belongs to the class of aldehydes. It has a molecular formula of C10H9N3O and a molecular weight of 187.2 g/mol. This yellow crystalline solid has a melting point of 159-160 °C and is commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It also has potential applications in the field of organic chemistry, where it can be used as a reagent for various chemical reactions. Additionally, 5-(2-FURYL)-1-METHYL-1H-PYRAZOLE-3-CARBALDEHYDE is known to have biological activities, but further research is needed to fully understand its potential uses in medicine and other fields.
Uses
Used in Pharmaceutical Industry:
5-(2-FURYL)-1-METHYL-1H-PYRAZOLE-3-CARBALDEHYDE is used as an intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of new drugs.
Used in Agrochemical Industry:
5-(2-FURYL)-1-METHYL-1H-PYRAZOLE-3-CARBALDEHYDE is used as an intermediate in the synthesis of agrochemicals to help create effective products for agricultural applications.
Used in Organic Chemistry:
5-(2-FURYL)-1-METHYL-1H-PYRAZOLE-3-CARBALDEHYDE is used as a reagent in various chemical reactions, playing a crucial role in advancing research and development in the field of organic chemistry.
Used in Research and Development:
5-(2-FURYL)-1-METHYL-1H-PYRAZOLE-3-CARBALDEHYDE is used in research and development for its potential biological activities, with ongoing studies aimed at understanding its full potential in medicine and other fields.
Check Digit Verification of cas no
The CAS Registry Mumber 876728-40-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,6,7,2 and 8 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 876728-40:
(8*8)+(7*7)+(6*6)+(5*7)+(4*2)+(3*8)+(2*4)+(1*0)=224
224 % 10 = 4
So 876728-40-4 is a valid CAS Registry Number.
InChI:InChI=1/C9H8N2O2/c1-11-8(5-7(6-12)10-11)9-3-2-4-13-9/h2-6H,1H3
876728-40-4Relevant articles and documents
Synthesis of new fluorinated tebufenpyrad analogs with acaricidal activity through regioselective pyrazole formation
Fustero, Santos,Roman, Raquel,Sanz-Cervera, Juan F.,Simon-Fuentes, Antonio,Bueno, Jorge,Villanova, Salvador
experimental part, p. 8545 - 8552 (2009/04/05)
(Chemical Equation Presented) In previous studies, our group has shown that the use of fluorinated alcohols such as trifluoroethanol (TFE) and hexafluoroisopropanol (HFIP) as solvents dramatically increases the regioselectivity in the pyrazole formation from 1,3-diketone with methylhydrazine. We have now applied this synthetic method to the preparation of new fluorinated pyrazoles, which have then been used as synthetic intermediates in the preparation of fluorinated analogs of Tebufenpyrad, a commercial acaricide. These compounds display a strong acaricidal activity that is either comparable to or better than that of the commercial compound.
