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CAS 850567-40-7

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B-[3-[[Bis(1-methylethyl)amino]carbonyl]phenyl]boronic acid

Description:
B-[3-[[Bis(1-methylethyl)amino]carbonyl]phenyl]boronic acid, with the CAS number 850567-40-7, is a boronic acid derivative characterized by its unique structural features that include a boron atom bonded to a phenyl group and an amino carbonyl substituent. 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 bis(1-methylethyl)amino group enhances its solubility and reactivity, potentially influencing its biological activity. Boronic acids are known for their role in drug development, particularly in the design of proteasome inhibitors and other therapeutic agents. Additionally, this compound may exhibit specific reactivity patterns due to the electron-donating nature of the amino group, which can affect its interaction with biological targets. Overall, B-[3-[[Bis(1-methylethyl)amino]carbonyl]phenyl]boronic acid represents a versatile building block in chemical research and development.
Formula:C13H20BNO3
InChI:InChI=1S/C13H20BNO3/c1-9(2)15(10(3)4)13(16)11-6-5-7-12(8-11)14(17)18/h5-10,17-18H,1-4H3
InChI key:InChIKey=WNUHFLVEXCGDIK-UHFFFAOYSA-N
SMILES:C(N(C(C)C)C(C)C)(=O)C1=CC(B(O)O)=CC=C1
Synonyms:
  • B-[3-[[Bis(1-methylethyl)amino]carbonyl]phenyl]boronic acid
  • Boronic acid, [3-[[bis(1-methylethyl)amino]carbonyl]phenyl]-
  • [3-(Diisopropylcarbamoyl)phenyl]boronic acid
  • Boronic acid, B-[3-[[bis(1-methylethyl)amino]carbonyl]phenyl]-
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