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CAS 1072951-85-9

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B-(6-Bromo-2-fluoro-3-propoxyphenyl)boronic acid

Description:
B-(6-Bromo-2-fluoro-3-propoxyphenyl)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 chemical reactions, particularly in Suzuki coupling reactions. The compound features a phenyl ring substituted with a bromine atom and a fluorine atom, which can influence its reactivity and solubility. The propoxy group enhances its lipophilicity, potentially affecting its biological activity and interactions. Boronic acids are often utilized in medicinal chemistry for drug development and in materials science for the synthesis of polymers. The presence of halogen substituents can also impart unique electronic properties, making this compound of interest in the development of novel materials and pharmaceuticals. Overall, B-(6-Bromo-2-fluoro-3-propoxyphenyl)boronic acid exhibits characteristics typical of boronic acids, including reactivity, solubility variations, and potential applications in organic synthesis and medicinal chemistry.
Formula:C9H11BBrFO3
InChI:InChI=1S/C9H11BBrFO3/c1-2-5-15-7-4-3-6(11)8(9(7)12)10(13)14/h3-4,13-14H,2,5H2,1H3
InChI key:InChIKey=NRFJKFUWHJKBRV-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(F)C(OCCC)=CC=C1Br
Synonyms:
  • Boronic acid, B-(6-bromo-2-fluoro-3-propoxyphenyl)-
  • B-(6-Bromo-2-fluoro-3-propoxyphenyl)boronic acid
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