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CAS 397843-70-8

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B-[3-[(Butylamino)carbonyl]phenyl]boronic acid

Description:
B-[3-[(Butylamino)carbonyl]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 butylamino carbonyl group, which enhances its solubility and reactivity. Its boronic acid moiety allows for participation in Suzuki-Miyaura cross-coupling reactions, a key method for forming carbon-carbon bonds in organic synthesis. Additionally, the presence of the butylamino group may impart specific biological activities, potentially making this compound of interest in drug development. The compound is typically handled with care due to the reactivity of boronic acids, particularly in the presence of moisture, which can lead to hydrolysis. Overall, B-[3-[(Butylamino)carbonyl]phenyl]boronic acid is a versatile compound with significant implications in both synthetic and medicinal chemistry.
Formula:C11H16BNO3
InChI:InChI=1/C11H16BNO3/c1-2-3-7-13-11(14)9-5-4-6-10(8-9)12(15)16/h4-6,8,15-16H,2-3,7H2,1H3,(H,13,14)
InChI key:InChIKey=UMTGJEHDHSYNMS-UHFFFAOYSA-N
SMILES:C(NCCCC)(=O)C1=CC(B(O)O)=CC=C1
Synonyms:
  • 3-(Butylaminocarbonyl)benzeneboronic acid
  • B-[3-[(Butylamino)carbonyl]phenyl]boronic acid
  • Boronic acid, B-[3-[(butylamino)carbonyl]phenyl]-
  • Boronic acid, [3-[(butylamino)carbonyl]phenyl]-
  • [3-(Butylcarbamoyl)Phenyl]Boronic Acid
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