847818-75-1 Usage
Uses
Used in Pharmaceutical Industry:
1-(2-Methylpropyl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1h-pyrazole is used as a building block for the synthesis of various pharmaceuticals. Its unique structure and biological activity make it a valuable component in the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical industry, 1-(2-Methylpropyl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1h-pyrazole serves as a key component in the synthesis of agrochemicals. Its versatility and reactivity contribute to the creation of effective compounds for agricultural applications.
Used in Catalysis:
1-(2-Methylpropyl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1h-pyrazole is utilized in catalysis due to its boron-containing structure. This unique feature allows it to act as a catalyst or a catalyst precursor in various chemical reactions, enhancing the efficiency and selectivity of the processes.
Used in Material Science:
In the field of material science, 1-(2-Methylpropyl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1h-pyrazole is employed for its potential applications in the development of new materials. Its distinct properties can contribute to the creation of advanced materials with specific characteristics for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 847818-75-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,7,8,1 and 8 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 847818-75:
(8*8)+(7*4)+(6*7)+(5*8)+(4*1)+(3*8)+(2*7)+(1*5)=221
221 % 10 = 1
So 847818-75-1 is a valid CAS Registry Number.
InChI:InChI=1/C13H23BN2O2/c1-10(2)9-16-11(7-8-15-16)14-17-12(3,4)13(5,6)18-14/h7-8,10H,9H2,1-6H3
847818-75-1Relevant academic research and scientific papers
Synthesis of pinacol esters of 1-alkyl-1H-pyrazol-5-yl- and 1-alkyl-1H-pyrazol-4-ylboronic acids
Ivachtchenko, Alexandre V.,Kravchenko, Dmitry V.,Zheludeva, Valentina I.,Pershin, Dmitry G.
, p. 931 - 939 (2007/10/03)
Starting from 1H-pyrazol, a wide number of 1-alkyl-1H-pyrazol-4-yl and 1-alkyl-1H-pyrazol-5-ylboronic acids and their pinacol esters were synthesized and characterized. The key step in the described methodology is the regioselective lithiation of the pyrazole ring. The synthesized pinacolates are stable under prolonged storage and can be used as convenient reagents in organic synthesis.
