B-(1-Phenyl-1H-pyrazol-4-yl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl-substituted pyrazole ring. This compound typically exhibits properties such as moderate solubility in polar organic solvents and can participate in various chemical reactions, including Suzuki coupling, which is significant in organic synthesis and medicinal chemistry. The boronic acid moiety allows for reversible interactions with diols, making it useful in biological applications, particularly in the development of sensors and drug delivery systems. Additionally, the pyrazole ring contributes to the compound's potential biological activity, as pyrazole derivatives are known for their diverse pharmacological properties. The compound's stability and reactivity can be influenced by factors such as pH and the presence of other functional groups. Overall, B-(1-Phenyl-1H-pyrazol-4-yl)boronic acid serves as a valuable building block in synthetic chemistry and has potential applications in various fields, including pharmaceuticals and materials science.

B-(1-Phenyl-1H-pyrazol-4-yl)boronic acid

1201643-70-0: Boronic acid, B-(1-phenyl-1H-pyrazol-4-yl)-, (1-Phenyl-1H-pyrazol-4-yl)boronicacid, B-(1-Phenyl-1H-pyrazol-4-yl)boronic acid, 1-Phenyl-1H-pyrazole-4-boronic acid, (1-Phenyl-1H-pyrazol-4-yl)boronic acid

1-Phenylpyrazole-4-boronic acid

Boronic acid, B-(1-phenyl-1H-pyrazol-4-yl)-

(1-Phenyl-1H-pyrazol-4-yl)boronic acid

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CAS 1201643-70-0: B-(1-Phenyl-1H-pyrazol-4-yl)boronic acid

1-Phenylpyrazole-4-boronic acid

Ref: 54-OR361529

Boronic acid, B-(1-phenyl-1H-pyrazol-4-yl)-

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(1-Phenyl-1H-pyrazol-4-yl)boronic acid

Ref: 10-F217442

(1-Phenyl-1H-pyrazol-4-yl)boronic acid

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