2644-94-2 Usage
Description
1-Benzyl-3,5-dimethyl-1H-pyrazole-4-carbaldehyde is a complex chemical compound that belongs to the class of pyrazole derivatives. It is a yellow solid substance with a unique molecular structure that makes it an important building block in the development of new drugs and biologically active compounds.
Uses
Used in Pharmaceutical Industry:
1-Benzyl-3,5-dimethyl-1H-pyrazole-4-carbaldehyde is used as an intermediate in the synthesis of pharmaceuticals and organic compounds. Its ability to interact with biological molecules and exhibit pharmacological activities makes it a promising candidate for the development of new drugs and medicinal compounds.
Used in Medicinal Chemistry:
1-Benzyl-3,5-dimethyl-1H-pyrazole-4-carbaldehyde is used as a building block in medicinal chemistry for the development of new drugs and biologically active compounds. Its unique structure allows for the creation of compounds with specific properties and functions that can be applied in various therapeutic areas.
Used in Industrial Applications:
1-Benzyl-3,5-dimethyl-1H-pyrazole-4-carbaldehyde has potential applications in the synthesis of materials with specific properties and functions in various industrial applications. Its unique structure and properties make it a valuable component in the development of innovative materials for different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 2644-94-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,4 and 4 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2644-94:
(6*2)+(5*6)+(4*4)+(3*4)+(2*9)+(1*4)=92
92 % 10 = 2
So 2644-94-2 is a valid CAS Registry Number.
InChI:InChI=1/C13H14N2O/c1-10-13(9-16)11(2)15(14-10)8-12-6-4-3-5-7-12/h3-7,9H,8H2,1-2H3
2644-94-2Relevant articles and documents
2-(pyrazol-4-yl)-1,3-oxaselenolanes from pyrazole carbaldehydes and 2-selanyl-1-ethanol
Papernaya, Lyubov K.,Shatrova, Alexandra A.,Levanova, Ekaterina P.,Albanov, Alexandr I.,Klyba, Lyudmila V.,Rudyakova, Elena V.,Levkovskaya, Galina G.
, p. 5 - 11 (2015/03/03)
Pyrazole carbaldehydes react with 2-selanyl-1-ethanol at room temperature in the presence of trimethylchlorosilane followed by treatment C with triethyl amine to afford the corresponding 2-(pyrazol-4-yl)-1,3-oxaselenolanes. The structure of the novel compounds was confirmed by IR, 13 C, 1 H, 15N, and 77 Se NMR spectroscopy.this article online at wileyonlinelibrary.com.
Fragmentation of pyrazolecarbaldehyde thio- and dithioacetals under electron impact and chemical ionization
Klyba,Papernaya,Sanzheeva,Shatrova,Rudyakova,Levkovskaya
body text, p. 1851 - 1858 (2012/03/11)
The mass spectra of 1-substituted 3,5-dimethyl-1H-pyrazole-4-carbaldehyde bis(2-hydroxyethyl) dithioacetals and thioacetals were studied for the first time. The main fragmentation pathways of their molecular ions generated under electron impact and chemic
2-[4-(PYRAZOL-4-YLALKYL)PIPERAZIN-1-YL]-3-PHENYL PYRAZINES AND PYRIDINES AND 3-[4-(PYRAZOL-4-YLALKYL)PIPERAZIN-1-YL]-2-PHENYL PYRIDINES AS 5-HT7 RECEPTOR ANTAGONISTS
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Page/Page column 55, (2009/01/20)
The present invention provides selective 5-HT7 receptor antagonist compounds of Formula I and their use in the treatment of migraine, persistent pain, and anxiety: where A and B are each independently C(H)= or N=, provided that at least one of A and B is -N=, n is 1-3, m is 0-3, and R14 are as defined herein.