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CAS 685103-98-4

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4-Isoquinolineboronic acid pinacol ester

Description:
4-Isoquinolineboronic acid pinacol ester is an organoboron compound characterized by the presence of a boronic acid functional group attached to an isoquinoline moiety. This compound typically exhibits a white to off-white solid appearance and is soluble in organic solvents such as dichloromethane and ethanol, but may have limited solubility in water. The boronic ester functionality allows for participation in various chemical reactions, particularly in Suzuki-Miyaura cross-coupling reactions, making it valuable in organic synthesis and medicinal chemistry. Its isoquinoline structure contributes to its potential biological activity, as isoquinolines are known for their diverse pharmacological properties. The compound is often used as a building block in the synthesis of more complex molecules, including pharmaceuticals and agrochemicals. Safety data sheets should be consulted for handling and storage guidelines, as with all chemical substances, to ensure proper safety measures are taken during use.
Formula:C15H20BNO3
InChI:InChI=1/C15H18BNO2/c1-14(2)15(3,4)19-16(18-14)13-10-17-9-11-7-5-6-8-12(11)13/h5-10H,1-4H3
SMILES:CC1(C)C(C)(C)OB(c2cncc3ccccc23)O1
Synonyms:
  • 4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)isoquinoline
  • 4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolane-2-yl)isoquinoline
  • 2-(4-Isoquinolyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
  • 4-ISOQUINOLINEBORONIC ACID, PINACOL ESTER
  • ISOQUINOLINE-4-BORONIC ACID, PINACOL ESTER
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