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CAS 874289-50-6

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[5-(butylcarbamoyl)-2-fluoro-phenyl]boronic acid

Description:
[5-(Butylcarbamoyl)-2-fluoro-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 and is widely used in organic synthesis and medicinal chemistry. The compound features a phenyl ring substituted with a fluoro group and a butylcarbamoyl moiety, which contributes to its solubility and reactivity. The presence of the boronic acid group allows for participation in Suzuki coupling reactions, making it valuable in the synthesis of complex organic molecules. Additionally, the fluoro substituent can influence the electronic properties of the molecule, potentially enhancing its biological activity or selectivity in various applications. The compound's structure suggests it may exhibit moderate to high polarity, affecting its solubility in different solvents. Overall, [5-(butylcarbamoyl)-2-fluoro-phenyl]boronic acid is a versatile building block in chemical synthesis, particularly in the development of pharmaceuticals and agrochemicals.
Formula:C11H15BFNO3
InChI:InChI=1/C11H15BFNO3/c1-2-3-6-14-11(15)8-4-5-10(13)9(7-8)12(16)17/h4-5,7,16-17H,2-3,6H2,1H3,(H,14,15)
SMILES:CCCCN=C(c1ccc(c(c1)B(O)O)F)O
Synonyms:
  • [5-(Butylcarbamoyl)-2-fluorophenyl]boronic acid
  • boronic acid, B-[5-[(butylamino)carbonyl]-2-fluorophenyl]-
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