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CAS 1256345-55-7

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B-[2-(Ethylthio)-5-(trifluoromethyl)-3-pyridinyl]boronic acid

Description:
B-[2-(Ethylthio)-5-(trifluoromethyl)-3-pyridinyl]boronic acid is a boronic acid derivative characterized by its unique functional groups and structural features. This compound contains a pyridine ring substituted with an ethylthio group and a trifluoromethyl group, which contribute to its chemical reactivity and potential applications in medicinal chemistry and organic synthesis. The boronic acid functional group is known for its ability to form reversible covalent bonds with diols, making it valuable in various chemical reactions, including Suzuki coupling reactions. The presence of the trifluoromethyl group enhances the lipophilicity and biological activity of the compound, while the ethylthio moiety may influence its solubility and interaction with biological targets. Overall, this compound's distinctive structure suggests potential utility in drug development, particularly in the design of inhibitors or modulators for specific biological pathways. Its CAS number, 1256345-55-7, allows for precise identification and retrieval of information related to its properties and applications in scientific literature.
Formula:C8H9BF3NO2S
InChI:InChI=1S/C8H9BF3NO2S/c1-2-16-7-6(9(14)15)3-5(4-13-7)8(10,11)12/h3-4,14-15H,2H2,1H3
InChI key:InChIKey=CAMZNTNANGCVOZ-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(SCC)N=CC(C(F)(F)F)=C1
Synonyms:
  • B-[2-(Ethylthio)-5-(trifluoromethyl)-3-pyridinyl]boronic acid
  • Boronic acid, B-[2-(ethylthio)-5-(trifluoromethyl)-3-pyridinyl]-
  • 2-(Ethylthio)-5-(trifluoromethyl)pyridin-3-ylboronic acid
  • 2-Ethylthio-5-trifluoromethylpyridine-3-boronic acid
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