847818-68-2 Usage
Uses
Used in Pharmaceutical Synthesis:
1,3-Dimethyl-1H-pyrazol-5-ylboronic acid is utilized as a key intermediate in the synthesis of pharmaceuticals, leveraging its reactivity to form stable complexes with electron-rich species, which is instrumental in the creation of new medicinal compounds.
Used in Organic Synthesis:
In the field of organic synthesis, 1,3-Dimethyl-1H-pyrazol-5-ylboronic acid serves as a versatile building block, contributing to the development of a diverse array of organic compounds due to its ability to engage in stable complex formations.
Used in Medicinal Chemistry:
1,3-Dimethyl-1H-pyrazol-5-ylboronic acid is employed as a reagent in medicinal chemistry, where its unique properties are harnessed to facilitate the discovery and optimization of potential drug candidates.
Used in Material Science:
1,3-Dimethyl-1H-pyrazol-5-ylboronic acid is also used in material science applications, where its chemical properties can be exploited to engineer new materials with specific characteristics, such as those with enhanced stability or reactivity.
Check Digit Verification of cas no
The CAS Registry Mumber 847818-68-2 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, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 847818-68:
(8*8)+(7*4)+(6*7)+(5*8)+(4*1)+(3*8)+(2*6)+(1*8)=222
222 % 10 = 2
So 847818-68-2 is a valid CAS Registry Number.
InChI:InChI=1S/C5H9BN2O2/c1-4-3-5(6(9)10)8(2)7-4/h3,9-10H,1-2H3
847818-68-2Relevant 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.
