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CAS 871332-72-8

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B-[4-Chloro-3-[[(1,1-dimethylethyl)amino]carbonyl]phenyl]boronic acid

Description:
B-[4-Chloro-3-[[(1,1-dimethylethyl)amino]carbonyl]phenyl]boronic acid, with the CAS number 871332-72-8, is a boronic acid derivative characterized by its boron atom bonded to a phenyl group that is further substituted with a chloro group and an amide functional group. 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 chloro substituent can influence its reactivity and solubility, while the tert-butylamino carbonyl group may enhance its stability and biological activity. Boronic acids are often utilized in the development of pharmaceuticals, particularly in the design of protease inhibitors and in the field of drug delivery systems. Additionally, this compound may exhibit specific interactions with biological targets, making it of interest in research related to cancer therapy and other diseases. Its unique structure and functional groups contribute to its potential utility in various chemical and biological applications.
Formula:C11H15BClNO3
InChI:InChI=1S/C11H15BClNO3/c1-11(2,3)14-10(15)8-6-7(12(16)17)4-5-9(8)13/h4-6,16-17H,1-3H3,(H,14,15)
InChI key:InChIKey=IKECDENKFPRPDM-UHFFFAOYSA-N
SMILES:C(NC(C)(C)C)(=O)C1=CC(B(O)O)=CC=C1Cl
Synonyms:
  • (3-(tert-Butylcarbamoyl)-4-chlorophenyl)boronicacid
  • B-[4-Chloro-3-[[(1,1-dimethylethyl)amino]carbonyl]phenyl]boronic acid
  • Boronic acid, [4-chloro-3-[[(1,1-dimethylethyl)amino]carbonyl]phenyl]-
  • Boronicacid, [4-chloro-3-[[(1,1-dimethylethyl)amino]carbonyl]phenyl]- (9CI)
  • Boronic acid, B-[4-chloro-3-[[(1,1-dimethylethyl)amino]carbonyl]phenyl]-
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