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CAS 269410-05-1

:

2-(2-Methoxy-1-naphthalenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Description:
2-(2-Methoxy-1-naphthalenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is an organoboron compound characterized by its unique boron-containing dioxaborolane structure, which contributes to its reactivity and utility in organic synthesis. This compound features a naphthalene moiety substituted with a methoxy group, enhancing its electronic properties and solubility in organic solvents. The presence of the dioxaborolane ring provides a stable boron atom that can participate in various chemical reactions, such as Suzuki coupling, making it valuable in the synthesis of complex organic molecules, particularly in the development of pharmaceuticals and materials science. Additionally, the tetramethyl substitution on the dioxaborolane ring increases steric hindrance, which can influence the compound's reactivity and selectivity in chemical transformations. Overall, this compound exemplifies the versatility of boron chemistry in facilitating the formation of carbon-carbon bonds and its application in advanced organic synthesis.
Formula:C17H21BO3
InChI:InChI=1S/C17H21BO3/c1-16(2)17(3,4)21-18(20-16)15-13-9-7-6-8-12(13)10-11-14(15)19-5/h6-11H,1-5H3
InChI key:InChIKey=RRKMZUYCRQLYHV-UHFFFAOYSA-N
SMILES:O(C)C1=C(C2=C(C=C1)C=CC=C2)B3OC(C)(C)C(C)(C)O3
Synonyms:
  • 2-(2-Methoxy-1-naphthalenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
  • 1,3,2-Dioxaborolane, 2-(2-methoxy-1-naphthalenyl)-4,4,5,5-tetramethyl-
  • 2-(2-Methoxynaphthalen-1-yl)-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane
  • 2-Methoxy-1-naphthaleneboronic acid pinacol ester
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