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CAS 871332-80-8

:

[3-(morpholine-4-carbonyl)-5-nitro-phenyl]boronic acid

Description:
[3-(Morpholine-4-carbonyl)-5-nitro-phenyl]boronic acid is a boronic acid derivative characterized by its unique functional groups, which include a morpholine ring, a nitro group, and a boronic acid moiety. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The presence of the nitro group can enhance its reactivity and influence its electronic properties, while the morpholine ring may contribute to its solubility and biological activity. Generally, boronic acids are known for their role in Suzuki coupling reactions, which are essential in the formation of carbon-carbon bonds. Additionally, this compound may exhibit potential biological activity, making it a candidate for further research in drug development. Its stability, solubility, and reactivity can vary based on the specific conditions and solvents used in experiments.
Formula:C11H13BN2O6
InChI:InChI=1/C11H13BN2O6/c15-11(13-1-3-20-4-2-13)8-5-9(12(16)17)7-10(6-8)14(18)19/h5-7,16-17H,1-4H2
InChI key:InChIKey=GKGNPJBVECYLOT-UHFFFAOYSA-N
SMILES:C1COCCN1C(=O)c1cc(cc(c1)N(=O)=O)B(O)O
Synonyms:
  • (3-(Morpholine-4-carbonyl)-5-nitrophenyl)boronic acid
  • B-[3-(4-Morpholinylcarbonyl)-5-nitrophenyl]boronic acid
  • Boronic acid, [3-(4-morpholinylcarbonyl)-5-nitrophenyl]-
  • [3-(Morpholin-4-ylcarbonyl)-5-nitrophenyl]boronic acid
  • boronic acid, B-[3-(4-morpholinylcarbonyl)-5-nitrophenyl]-
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