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CAS 871329-57-6

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[3-(tert-butoxycarbonylamino)-4-chloro-phenyl]boronic acid

Description:
[3-(tert-butoxycarbonylamino)-4-chloro-phenyl]boronic acid is a boronic acid derivative characterized by the presence of a boron atom bonded to a phenyl group that is substituted with a chloro group and a tert-butoxycarbonylamino group. This compound typically exhibits properties common to boronic acids, such as the ability to form reversible complexes with diols, making it useful in various organic synthesis applications, particularly in Suzuki coupling reactions. The tert-butoxycarbonyl (Boc) group serves as a protecting group for amines, allowing for selective reactions without affecting the amine functionality. The presence of the chloro substituent can influence the reactivity and solubility of the compound. In terms of physical properties, boronic acids generally have moderate solubility in polar solvents and can exhibit acidic behavior due to the presence of the boronic acid functional group. This compound may also be of interest in medicinal chemistry for its potential applications in drug development and as a building block in the synthesis of more complex molecules.
Formula:C11H15BClNO4
InChI:InChI=1/C11H15BClNO4/c1-11(2,3)18-10(15)14-9-6-7(12(16)17)4-5-8(9)13/h4-6,16-17H,1-3H3,(H,14,15)
SMILES:CC(C)(C)OC(=Nc1cc(ccc1Cl)B(O)O)O
Synonyms:
  • 3-AMINO-4-CHLOROBENZENEBORONIC ACID, N-BOC PROTECTED
  • N-BOC-3-AMINO-4-CHLOROBENZENEBORONIC ACID
  • 3-(TERT-BUTOXYCARBONYLAMINO)-4-CHLOROPHENYLBORONIC ACID
  • 3-Amino-4-chlorobenzeneboronic acid, N-BOC protected 97%
  • 3-BOC-AMINO-4-CHLOROPHENYLBORONIC ACID
  • 3-(tert-Butoxycarbonylamino)-4-chlorobenzeneboronic acid
  • Carbamic acid, N-(5-borono-2-chlorophenyl)-, C-(1,1-dimethylethyl) ester
  • 3-(Boc-aMino)-4-chlorobenzeneboronic acid, 97%
  • 3-(t-Butoxycarbonylamino)-4-chlorophenylboronic acid
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