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CAS 1889221-15-1

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Boronic acid, B-[6-methyl-5-(trifluoromethyl)-3-pyridinyl]-

Description:
Boronic acid, specifically B-[6-methyl-5-(trifluoromethyl)-3-pyridinyl]- (CAS 1889221-15-1), is an organoboron compound characterized by the presence of a boronic acid functional group (-B(OH)2) attached to a pyridine ring. This compound features a trifluoromethyl group, which enhances its lipophilicity and can influence its reactivity and biological activity. The methyl group on the pyridine ring can also affect the electronic properties of the molecule. Boronic acids are known for their ability to form reversible covalent bonds with diols, making them valuable in various applications, including organic synthesis and medicinal chemistry. They are often utilized in the development of pharmaceuticals and agrochemicals due to their ability to act as intermediates in cross-coupling reactions, such as Suzuki-Miyaura coupling. Additionally, the presence of fluorine atoms can impart unique properties, such as increased metabolic stability and altered pharmacokinetics. Overall, this compound exemplifies the diverse functionality and utility of boronic acids in chemical research and application.
Formula:C7H7BF3NO2
InChI:InChI=1S/C7H7BF3NO2/c1-4-6(7(9,10)11)2-5(3-12-4)8(13)14/h2-3,13-14H,1H3
InChI key:InChIKey=BPTCKBBULUZEIR-UHFFFAOYSA-N
SMILES:C(F)(F)(F)C=1C=C(B(O)O)C=NC1C
Synonyms:
  • [6-Methyl-5-(trifluoromethyl)pyridin-3-yl]boronic acid
  • Boronic acid, B-[6-methyl-5-(trifluoromethyl)-3-pyridinyl]-
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