4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1-naphthalenecarboxaldehyde

For research use only. Not for therapeutic Use.

  • CAT Number: L002907
  • CAS Number: 1008361-71-4
  • Molecular Formula: C17H19BO3
  • Molecular Weight: 282.10
  • Purity: ≥95%
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4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1-naphthalenecarboxaldehyde(Cat No.:L002907)is a boronic ester derivative featuring a naphthalenecarboxaldehyde core and a dioxaborolane moiety. This compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to form carbon-carbon bonds. Its boronic ester group provides reactivity that allows for the construction of complex molecular architectures, making it valuable in the development of pharmaceuticals, fine chemicals, and materials science. Researchers utilize this compound in medicinal chemistry for creating novel drug candidates and exploring advanced synthetic pathways.


Catalog Number L002907
CAS Number 1008361-71-4
Molecular Formula C17H19BO3
Purity ≥95%
IUPAC Name 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)naphthalene-1-carbaldehyde
InChI InChI=1S/C17H19BO3/c1-16(2)17(3,4)21-18(20-16)15-10-9-12(11-19)13-7-5-6-8-14(13)15/h5-11H,1-4H3
InChIKey JYOLGAMKDPDGSG-UHFFFAOYSA-N
SMILES B1(OC(C(O1)(C)C)(C)C)C2=CC=C(C3=CC=CC=C23)C=O

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