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CS-W001157 4
Total: USD 88.00

4,4,5,5-Tetramethyl-2-(triphenylen-2-yl)-1,3,2-dioxaborolane

  • CAS No. 890042-13-4

  • Cat. No. CS-0153833
  • Purity≥97%
  • MDL No.MFCD26401844

*For research and further manufacturing use only, not for direct human use.

4,4,5,5-Tetramethyl-2-(triphenylen-2-yl)-1,3,2-dioxaborolane|CS-0153833

Structure of 890042-13-4

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General Information

  • CAS No. 890042-13-4
  • Cat. No. CS-0153833
  • Purity ≥97%
  • MDL No. MFCD26401844
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₂₄H₂₃BO₂
  • Molecular Weight 354.25
  • Synonym(s) Triphenylen-2-ylboronic Acid Pinacol Ester
  • SMILES CC1(C)C(C)(C)OB(C2=CC3=C(C=C2)C4=CC=CC=C4C5=CC=CC=C53)O1

Description

This boronate ester features a triphenylenyl group integrated at the 2-position, enhancing electronic delocalization and stability. The tetramethyl-substituted dioxaborolane ring ensures excellent bench stability and moisture tolerance, enabling reliable use in Suzuki-Miyaura cross-coupling reactions under standard conditions.

Application

4,4,5,5-Tetramethyl-2-(triphenylen-2-yl)-1,3,2-dioxaborolane serves as a stable, bench-ready boron source for Suzuki-Miyaura cross-coupling reactions. Its triphenylenyl moiety imparts enhanced planarity and electronic stability, enabling efficient coupling with aryl halides and pseudohalides under standard conditions. The tetramethyl substitution ensures excellent shelf life and ease of handling, while the dioxaborolane ring facilitates clean reaction profiles and straightforward purification—ideal for constructing complex biaryl scaffolds in medicinal chemistry and materials science applications.

Safety Information

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GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H302-H315-H319-H335
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501

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Computational Chemistry Data

  • TPSA   18.46
  • LogP   5.4454
  • H_Acceptors   2
  • H_Donors   0
  • Rotatable_Bonds   1

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