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CAS 199609-62-6

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3-((N-BOC-AMINO)METHYL)PHENYLBORONIC ACID

Description:
3-((N-BOC-AMINO)METHYL)PHENYLBORONIC ACID, with the CAS number 199609-62-6, is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring. The compound features a tert-butoxycarbonyl (BOC) protected amino group, which enhances its stability and solubility in organic solvents. This structure allows for potential applications in medicinal chemistry, particularly in the development of boron-containing compounds for drug discovery and synthesis. The boronic acid moiety is known for its ability to form reversible covalent bonds with diols, making it useful in various chemical reactions, including Suzuki coupling reactions. The compound is typically a white to off-white solid and is soluble in polar organic solvents. Its reactivity and functional groups make it a valuable intermediate in organic synthesis, particularly in the preparation of biologically active molecules. Safety data should be consulted for handling and storage, as with all chemical substances.
Formula:C12H18BNO4
InChI:InChI=1/C12H18BNO4/c1-12(2,3)18-11(15)14-8-9-5-4-6-10(7-9)13(16)17/h4-7,16-17H,8H2,1-3H3,(H,14,15)
SMILES:CC(C)(C)OC(=NCc1cccc(c1)B(O)O)O
Synonyms:
  • 3-(Tert-Butoxycarbonylaminomethyl)Phenylboronic Acid
  • 3-(N-Boc-Aminomethyl)Benzeneboronic Acid
  • 3-(N-Tert-Butoxycarbonyl)Aminomethylphenyl Boronic Acid
  • 3-(Aminomethyl)benzeneboronic acid, N-BOC protected
  • 3-(Aminomethyl)benzeneboronic acid, N-BOC protected 97%
  • N-Boc-3-(Aminomethyl)Benzeneboronic Acid
  • (3-{[(Tert-Butoxycarbonyl)Amino]Methyl}Phenyl)Boronic Acid
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