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CAS 851883-08-4

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3,4-Diaminophenylboronicacid,pinacolester

Description:
3,4-Diaminophenylboronic acid pinacol ester is an organic compound characterized by the presence of both amine and boronic acid functional groups. The compound features a phenyl ring substituted with two amino groups at the 3 and 4 positions, which enhances its reactivity and potential for forming hydrogen bonds. The boronic acid moiety is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, including drug development and materials science. The pinacol ester group serves to stabilize the boronic acid, improving its solubility and reactivity in organic synthesis. This compound is typically utilized in the synthesis of complex organic molecules and in the development of sensors and catalysts. Its properties, such as solubility, stability, and reactivity, can be influenced by the presence of the pinacol ester and the amino groups, making it a versatile building block in organic chemistry. Safety and handling precautions should be observed, as with all chemical substances, due to potential hazards associated with amines and boron-containing compounds.
Formula:C12H19BN2O2
InChI:InChI=1S/C12H19BN2O2/c1-11(2)12(3,4)17-13(16-11)8-5-6-9(14)10(15)7-8/h5-7H,14-15H2,1-4H3
Synonyms:
  • 3,4-Diaminophenylboronic Acid Pinacol Ester
  • 4-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)Benzene-1,2-Diamine
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