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CAS 2096336-18-2

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B-[2-Fluoro-5-methyl-3-(1-methylethoxy)phenyl]boronic acid

Description:
B-[2-Fluoro-5-methyl-3-(1-methylethoxy)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 a fluorine atom and a branched alkoxy group, which can influence its reactivity and solubility. The presence of the methyl and ethoxy groups contributes to its hydrophobic characteristics, potentially affecting its interactions in biological systems. This compound may exhibit unique properties such as selective reactivity in cross-coupling reactions, making it valuable in the development of pharmaceuticals and agrochemicals. Additionally, the fluorine substitution can enhance the compound's metabolic stability and bioavailability. Overall, B-[2-Fluoro-5-methyl-3-(1-methylethoxy)phenyl]boronic acid represents a versatile building block in synthetic chemistry, particularly in the context of drug discovery and development.
Formula:C10H14BFO3
InChI:InChI=1S/C10H14BFO3/c1-6(2)15-9-5-7(3)4-8(10(9)12)11(13)14/h4-6,13-14H,1-3H3
InChI key:InChIKey=QFGYOSZZKDRXGM-UHFFFAOYSA-N
SMILES:O(C(C)C)C1=C(F)C(B(O)O)=CC(C)=C1
Synonyms:
  • Boronic acid, B-[2-fluoro-5-methyl-3-(1-methylethoxy)phenyl]-
  • B-[2-Fluoro-5-methyl-3-(1-methylethoxy)phenyl]boronic acid
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