
CAS 1308298-23-8
:[2-(Trifluoromethyl)pyrimidin-5-yl]boronic acid
Description:
[2-(Trifluoromethyl)pyrimidin-5-yl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a pyrimidine ring that features a trifluoromethyl substituent. This compound typically exhibits properties such as high thermal stability and solubility in polar organic solvents, making it useful in various chemical reactions, particularly in Suzuki-Miyaura cross-coupling reactions, which are essential for forming carbon-carbon bonds in organic synthesis. The trifluoromethyl group enhances the compound's lipophilicity and can influence its reactivity and biological activity. Additionally, boronic acids are known for their ability to form reversible complexes with diols, which can be exploited in sensor applications and drug design. The presence of the pyrimidine moiety may also impart specific biological activities, making this compound of interest in medicinal chemistry. Overall, [2-(Trifluoromethyl)pyrimidin-5-yl]boronic acid is a versatile building block in synthetic organic chemistry and pharmaceutical development.
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Found 3 products.
Boronic acid, B-[2-(trifluoromethyl)-5-pyrimidinyl]-
CAS:Formula:C5H4BF3N2O2Purity:95%Color and Shape:SolidMolecular weight:191.9037(2-(Trifluoromethyl)pyrimidin-5-yl)boronic acid
CAS:(2-(Trifluoromethyl)pyrimidin-5-yl)boronic acidPurity:95%Molecular weight:191.91g/mol(2-(Trifluoromethyl)pyrimidin-5-yl)boronic acid
CAS:Formula:C5H4BF3N2O2Purity:95%Color and Shape:SolidMolecular weight:191.9


