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CAS 871332-79-5

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B-[3-[(Ethylamino)carbonyl]-5-nitrophenyl]boronic acid

Description:
B-[3-[(Ethylamino)carbonyl]-5-nitrophenyl]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 nitrophenyl moiety, which contributes to its electronic properties and potential reactivity. The ethylamino carbonyl group enhances its solubility and may influence its biological activity. Typically, boronic acids exhibit moderate to high stability under ambient conditions but can be sensitive to moisture and air, necessitating careful handling and storage. This compound may also participate in Suzuki-Miyaura cross-coupling reactions, a key method in the formation of carbon-carbon bonds in organic synthesis. Its unique structure suggests potential applications in drug development, particularly in targeting specific biological pathways or as a building block in the synthesis of more complex molecules. As with all chemical substances, safety data sheets should be consulted for handling and toxicity information.
Formula:C9H11BN2O5
InChI:InChI=1S/C9H11BN2O5/c1-2-11-9(13)6-3-7(10(14)15)5-8(4-6)12(16)17/h3-5,14-15H,2H2,1H3,(H,11,13)
InChI key:InChIKey=FWBAGEDRZQWROK-UHFFFAOYSA-N
SMILES:C(NCC)(=O)C1=CC(B(O)O)=CC(N(=O)=O)=C1
Synonyms:
  • B-[3-[(Ethylamino)carbonyl]-5-nitrophenyl]boronic acid
  • Boronic acid, B-[3-[(ethylamino)carbonyl]-5-nitrophenyl]-
  • Boronic acid, [3-[(ethylamino)carbonyl]-5-nitrophenyl]-
  • [3-(Ethylcarbamoyl)-5-nitrophenyl]boronic acid
  • boronic acid, B-[3-[(ethylamino)carbonyl]-5-nitrophenyl]-(3-(Ethylcarbamoyl)-5-Nitrophenyl)Boronic Acid
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