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CAS 871332-89-7

:

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

Description:
B-[3-[(Butylamino)carbonyl]-5-nitrophenyl]boronic acid is an organic compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols. This compound features a nitrophenyl moiety, which contributes to its electronic properties and potential reactivity. The butylamino group enhances its solubility and may influence its biological activity, making it of interest in medicinal chemistry. The presence of the boronic acid group suggests potential applications in drug development, particularly in the design of inhibitors for enzymes like proteases or in the synthesis of complex organic molecules through Suzuki coupling reactions. Additionally, the compound's structure indicates it may exhibit unique interactions with biological targets, potentially leading to therapeutic applications. Its CAS number, 871332-89-7, allows for easy identification and reference in chemical databases. Overall, this compound exemplifies the intersection of organic synthesis and medicinal chemistry, highlighting the importance of functional group manipulation in developing new therapeutic agents.
Formula:C11H15BN2O5
InChI:InChI=1S/C11H15BN2O5/c1-2-3-4-13-11(15)8-5-9(12(16)17)7-10(6-8)14(18)19/h5-7,16-17H,2-4H2,1H3,(H,13,15)
InChI key:InChIKey=BXFORXWKNBRZNX-UHFFFAOYSA-N
SMILES:C(NCCCC)(=O)C1=CC(B(O)O)=CC(N(=O)=O)=C1
Synonyms:
  • 3-(N-Butylcarbamoyl)-5-Nitrophenylboronic Acid
  • 3-(N-Butylcarbamoyl)-5-Nitrophenylboronicacid
  • B-[3-[(Butylamino)carbonyl]-5-nitrophenyl]boronic acid
  • Boronic acid, [3-[(butylamino)carbonyl]-5-nitrophenyl]-
  • [3-(Butylcarbamoyl)-5-nitrophenyl]boronic acid
  • boronic acid, B-[3-[(butylamino)carbonyl]-5-nitrophenyl]-
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