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CAS 1704063-95-5

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B-[4-Fluoro-3-(4-morpholinylmethyl)phenyl]boronic acid

Description:
B-[4-Fluoro-3-(4-morpholinylmethyl)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 medicinal chemistry and organic synthesis. The compound features a phenyl ring substituted with a fluorine atom and a morpholinylmethyl group, which contributes to its biological activity and solubility properties. The morpholine moiety can enhance the compound's interaction with biological targets, potentially influencing its pharmacological profile. Additionally, the presence of the boronic acid group allows for participation in Suzuki coupling reactions, a key method in the formation of carbon-carbon bonds in organic synthesis. This compound may exhibit specific reactivity and selectivity due to its structural features, making it a candidate for further research in drug development and material science. Its CAS number, 1704063-95-5, uniquely identifies it in chemical databases, facilitating its study and application in various fields.
Formula:C11H15BFNO3
InChI:InChI=1S/C11H15BFNO3/c13-11-2-1-10(12(15)16)7-9(11)8-14-3-5-17-6-4-14/h1-2,7,15-16H,3-6,8H2
InChI key:InChIKey=GHABZEPGSYBSSW-UHFFFAOYSA-N
SMILES:C(C1=CC(B(O)O)=CC=C1F)N2CCOCC2
Synonyms:
  • Boronic acid, B-[4-fluoro-3-(4-morpholinylmethyl)phenyl]-
  • B-[4-Fluoro-3-(4-morpholinylmethyl)phenyl]boronic acid
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