cas 847818-56-8|| where to buy 1-Ethylpyrazole-4-boronic acid

Product Name:1-Ethylpyrazole-4-boronic acid

IUPAC Name:(1-ethyl-1H-pyrazol-4-yl)boronic acid

: CAS：847818-56-8; Molecular Formula：C5H9BN2O2; Purity：95%+

: Catalog Number：CM134104; Molecular Weight：139.95

Packing Unit	Available Stock	Price($)
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Product Details

: CAS NO:847818-56-8; Molecular Formula:C5H9BN2O2; Melting Point:-; Smiles Code:CCN1N=CC(B(O)O)=C1; Density:

: Catalog Number:CM134104; Molecular Weight:139.95; Boiling Point:322.9±34.0°C at 760 mmHg; MDL No:MFCD10703521; Storage:-20°C

Category Infos

: Pyrazoles; Pyrazoles are organic compounds of the general formula C3H3N2H. It is a five-membered heterocycle consisting of three carbon atoms and two adjacent nitrogen atoms. As an H-bond-donating heterocycle, pyrazole has been used as a more lipophilic and metabolically more stable bioisomer of phenol. Pyrazoles have attracted more and more attention due to their broad spectrum of action and strong efficacy.; Pyrazone; Custom pyrazone for customers from all over the world are our main business.

: Boronic Acids and Esters; Boronic acids and boronate esters are commonly used reagents in Suzuki–Miyaura coupling chemistry. Organoboron derivatives are common reagents for C–C bond formation, either through classical palladium-mediated transformations or through other newer coupling methods. Boronic esters and acids are potential intermediates in the manufacture of many active pharmaceutical ingredients (API).; Boronic Acid For Sale; Find trusted boronic acid for sale. Any requirements and problems can ask us at any time.

Column Infos

: Boronic Acids and Esters

Product Other Information

Product Overview	1-Ethylpyrazole-4-boronic acid (EPBA) is an organic compound that has recently gained attention for its potential applications in organic synthesis, medicinal chemistry, and biochemistry. EPBA is a versatile reagent and has been used in a variety of reactions, including Suzuki, Stille, and Heck couplings. EPBA is also used as a catalyst in the synthesis of complex molecules. In addition to its synthetic applications, EPBA has been studied for its potential biochemical and physiological effects.
Synthesis and Application	1-Ethylpyrazole-4-boronic acid can be synthesized in a variety of ways. The most common method involves the reaction of ethylpyrazole and boronic acid in the presence of a base such as potassium carbonate. The reaction proceeds through an SN2 mechanism and yields a mixture of the desired 1-Ethylpyrazole-4-boronic acid and the by-product, boric acid. The reaction can be optimized by controlling the reaction temperature, reaction time, and molar ratio of reactants. 1-Ethylpyrazole-4-boronic acid has been used in a variety of scientific research applications. It has been used as a reagent in organic synthesis to facilitate the formation of carbon-carbon bonds in the synthesis of complex molecules. 1-Ethylpyrazole-4-boronic acid has also been used in medicinal chemistry as a catalyst in the synthesis of bioactive compounds. In addition, 1-Ethylpyrazole-4-boronic acid has been used in biochemistry and molecular biology to study the action of enzymes and other protein targets.
Future Directions	The potential applications of 1-Ethylpyrazole-4-boronic acid are still being explored. Future research could focus on developing new synthetic methods for the synthesis of 1-Ethylpyrazole-4-boronic acid and other related compounds. Additionally, more research could be done to explore the biochemical and physiological effects of 1-Ethylpyrazole-4-boronic acid and to develop new methods for its use in medicinal chemistry and biochemistry. Finally, further research could be done to optimize the use of 1-Ethylpyrazole-4-boronic acid in organic synthesis and to develop new catalysts based on 1-Ethylpyrazole-4-boronic acid.