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CAS 871333-04-9

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B-[4-[(Ethylmethylamino)carbonyl]phenyl]boronic acid

Description:
B-[4-[(Ethylmethylamino)carbonyl]phenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which typically exhibits properties such as Lewis acidity and the ability to form reversible covalent bonds with diols. This compound features a phenyl ring substituted with an ethylmethylamino group and a carbonyl moiety, contributing to its potential biological activity and utility in medicinal chemistry. The boronic acid group allows for interactions with biomolecules, making it useful in drug development and as a tool in chemical biology, particularly in the context of targeting specific proteins or pathways. Additionally, boronic acids are known for their role in Suzuki coupling reactions, which are important in organic synthesis. The compound's solubility, stability, and reactivity can be influenced by the substituents on the phenyl ring and the nature of the boron atom. Overall, B-[4-[(Ethylmethylamino)carbonyl]phenyl]boronic acid represents a versatile structure with applications in various fields, including pharmaceuticals and materials science.
Formula:C10H14BNO3
InChI:InChI=1S/C10H14BNO3/c1-3-12(2)10(13)8-4-6-9(7-5-8)11(14)15/h4-7,14-15H,3H2,1-2H3
InChI key:InChIKey=AWXVNEUNYSIXAD-UHFFFAOYSA-N
SMILES:C(N(CC)C)(=O)C1=CC=C(B(O)O)C=C1
Synonyms:
  • B-[4-[(Ethylmethylamino)carbonyl]phenyl]boronic acid
  • Boronic acid, B-[4-[(ethylmethylamino)carbonyl]phenyl]-
  • Boronic acid, [4-[(ethylmethylamino)carbonyl]phenyl]-
  • [4-[Ethyl(methyl)carbamoyl]phenyl]boronic acid
  • (4-(Ethyl(methyl)carbamoyl)phenyl)boronic acid
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