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

For research use only. Not for therapeutic Use.

  • CAT Number: L045414
  • CAS Number: 380151-85-9
  • Molecular Formula: C13H17BO3
  • Molecular Weight: 232.09
  • Purity: ≥95%
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2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde(Cat No.:L045414)is a chemical compound featuring a benzaldehyde core substituted with a boronate ester group. The boronate ester, 4,4,5,5-tetramethyl-1,3,2-dioxaborolane, is known for its stability and reactivity in Suzuki coupling reactions, making this compound valuable in organic synthesis. It is commonly used as an intermediate for the formation of various biaryl structures, essential for creating complex molecules in pharmaceutical and materials chemistry. This compound finds utility in areas like drug discovery and chemical research due to its versatile reactivity and functional group compatibility.


CAS Number 380151-85-9
Molecular Formula C13H17BO3
Purity ≥95%
IUPAC Name 2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde
InChI InChI=1S/C13H17BO3/c1-12(2)13(3,4)17-14(16-12)11-8-6-5-7-10(11)9-15/h5-9H,1-4H3
InChIKey SLJMPQLPRHIAOM-UHFFFAOYSA-N
SMILES B1(OC(C(O1)(C)C)(C)C)C2=CC=CC=C2C=O
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