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CAS 1256345-87-5

:

B-[3-Ethoxy-5-(trifluoromethoxy)phenyl]boronic acid

Description:
B-[3-Ethoxy-5-(trifluoromethoxy)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 useful in various applications, including organic synthesis and medicinal chemistry. The compound features a phenyl ring substituted with an ethoxy group and a trifluoromethoxy group, which contribute to its unique chemical properties, such as increased lipophilicity and potential for enhanced reactivity. The trifluoromethoxy group, in particular, can influence the electronic properties of the molecule, potentially enhancing its reactivity in cross-coupling reactions. Additionally, boronic acids are often utilized in the development of pharmaceuticals and agrochemicals due to their ability to participate in Suzuki-Miyaura coupling reactions. The compound's solubility, stability, and reactivity can be influenced by the presence of these substituents, making it a valuable building block in synthetic chemistry. Overall, B-[3-Ethoxy-5-(trifluoromethoxy)phenyl]boronic acid exemplifies the versatility of boronic acids in chemical synthesis.
Formula:C9H10BF3O4
InChI:InChI=1S/C9H10BF3O4/c1-2-16-7-3-6(10(14)15)4-8(5-7)17-9(11,12)13/h3-5,14-15H,2H2,1H3
InChI key:InChIKey=CIBQUPSDYSPZER-UHFFFAOYSA-N
SMILES:O(C(F)(F)F)C1=CC(B(O)O)=CC(OCC)=C1
Synonyms:
  • Boronic acid, B-[3-ethoxy-5-(trifluoromethoxy)phenyl]-
  • B-[3-Ethoxy-5-(trifluoromethoxy)phenyl]boronic acid
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