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Welcome to Organoboron Compounds Database

Boronic acids and their esters are highly popular synthetic intermediates in organic synthesis for their ease and efficiency of conversion to other functional groups, in metal-catalyzed cross-coupling reactions and for their unique biochemical activity.

The palladium-catalyzed cross-coupling reaction of organoboron compounds with organic halides or pseudo-halides - the Suzuki-Miyaura reaction - is a remarkably useful tool in organic synthesis.

A new class of air-stable boronic acid derivatives is trifluoroborates, which are offering a unique alternative to most boronic acids, esters and organoboranes for use in Suzuki-Miyaura and other transition-metal-catalyzed cross-coupling reactions.

As inhibitors of serine proteases, boronic acids inhibit therapeutically relevant proteases and proteasomes. FDA has approved the first boron-containing drug, bortezomib (Velcade) for the treatment of multiple myeloma and mantle cell lymphoma.

A chemical database containing CAS number, synthesis references, physical properties (melting/boiling point, refractive index, density and solubility) for more than 2,000 boronic acids, boronic acid esters and trifluoroborates is available on our website.

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boronic acids
All boronic acids
Arylboronic acids
Arylboronic acids
Alkylboronic acids
Alkylboronic acids
Phenylboronic acid
Phenylboronic acid
Pyridineboronic acids
Pyridineboronic acids
Catechol boronic esters
Catechol esters
Ethylene glycol boronic esters
Ethylene glycol esters
Neopentyl glycol boronic esters
Neopentyl glycol esters
Pinacol boronic esters
Pinacol esters
Trifluoroborate Salts
Trifluoroborate Salts

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