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CAS 1072946-33-8

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B-[5-Chloro-2-methyl-4-(trifluoromethyl)phenyl]boronic acid

Description:
B-[5-Chloro-2-methyl-4-(trifluoromethyl)phenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols, making it valuable in various chemical reactions, particularly in Suzuki coupling reactions. This compound features a chlorinated aromatic ring, which enhances its reactivity and solubility in organic solvents. The trifluoromethyl group contributes to its electronic properties, often increasing lipophilicity and influencing its interaction with biological systems. The presence of the methyl group on the aromatic ring can affect steric hindrance and reactivity. As a boronic acid, it can participate in the formation of boronate esters, which are useful intermediates in organic synthesis. Additionally, compounds like this one are often studied for their potential applications in medicinal chemistry, particularly in the development of pharmaceuticals targeting specific biological pathways. Overall, B-[5-Chloro-2-methyl-4-(trifluoromethyl)phenyl]boronic acid is a versatile compound with significant implications in both synthetic and medicinal chemistry.
Formula:C8H7BClF3O2
InChI:InChI=1S/C8H7BClF3O2/c1-4-2-5(8(11,12)13)7(10)3-6(4)9(14)15/h2-3,14-15H,1H3
InChI key:InChIKey=WIXOOBHBVKOORA-UHFFFAOYSA-N
SMILES:C(F)(F)(F)C1=C(Cl)C=C(B(O)O)C(C)=C1
Synonyms:
  • [5-Chloro-2-methyl-4-(trifluoromethyl)phenyl]boronic acid
  • B-[5-Chloro-2-methyl-4-(trifluoromethyl)phenyl]boronic acid
  • Boronic acid, B-[5-chloro-2-methyl-4-(trifluoromethyl)phenyl]-
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