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CAS 849052-20-6

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

Description:
B-(2-Bromo-6-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 applications, particularly in organic synthesis and medicinal chemistry. The compound features a phenyl ring substituted with a bromine atom, a fluorine atom, and a propoxy group, contributing to its unique reactivity and potential biological activity. The presence of the boronic acid moiety allows for participation in Suzuki-Miyaura cross-coupling reactions, facilitating the formation of carbon-carbon bonds. Additionally, the halogen substituents can enhance the compound's lipophilicity and influence its interaction with biological targets. This compound may also exhibit properties relevant to drug development, particularly in the context of targeting specific enzymes or receptors. Overall, B-(2-Bromo-6-fluoro-3-propoxyphenyl)boronic acid is a versatile building block in synthetic chemistry with potential applications in pharmaceuticals and materials science.
Formula:C9H11BBrFO3
InChI:InChI=1/C9H11BBrFO3/c1-2-5-15-7-4-3-6(12)8(9(7)11)10(13)14/h3-4,13-14H,2,5H2,1H3
InChI key:InChIKey=AIRJDYNENADRSB-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(Br)C(OCCC)=CC=C1F
Synonyms:
  • Boronic acid, B-(2-bromo-6-fluoro-3-propoxyphenyl)-
  • B-(2-Bromo-6-fluoro-3-propoxyphenyl)boronic acid
  • Boronic acid, (2-bromo-6-fluoro-3-propoxyphenyl)-
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