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CAS 871332-88-6

:

B-[3-Nitro-5-[(propylamino)carbonyl]phenyl]boronic acid

Description:
B-[3-Nitro-5-[(propylamino)carbonyl]phenyl]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, making it useful in various applications, including medicinal chemistry and materials science. The compound features a nitro group and a propylamino carbonyl substituent on a phenyl ring, contributing to its potential biological activity and reactivity. The boronic acid moiety allows for participation in Suzuki coupling reactions, which are valuable in the synthesis of complex organic molecules. Additionally, the presence of the nitro group may influence the compound's electronic properties and solubility. This compound is typically used in research settings, particularly in the development of pharmaceuticals and as a building block in organic synthesis. Its specific properties, such as solubility, melting point, and reactivity, would depend on the conditions under which it is studied or utilized.
Formula:C10H13BN2O5
InChI:InChI=1/C10H13BN2O5/c1-2-3-12-10(14)7-4-8(11(15)16)6-9(5-7)13(17)18/h4-6,15-16H,2-3H2,1H3,(H,12,14)
InChI key:InChIKey=HNHYFGGDBCBQMF-UHFFFAOYSA-N
SMILES:C(NCCC)(=O)C1=CC(B(O)O)=CC(N(=O)=O)=C1
Synonyms:
  • B-[3-Nitro-5-[(propylamino)carbonyl]phenyl]boronic acid
  • Boronic acid, B-[3-nitro-5-[(propylamino)carbonyl]phenyl]-
  • Boronic acid, [3-nitro-5-[(propylamino)carbonyl]phenyl]-
  • boronic acid, B-[3-nitro-5-[(propylamino)carbonyl]phenyl]-(3-Nitro-5-(Propylcarbamoyl)Phenyl)Boronic Acid
  • [3-Nitro-5-(propylcarbamoyl)phenyl]boronic acid
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