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CS-W001157 4
Total: USD 88.00

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

  • CAS No. 475250-43-2

  • Cat. No. CS-W021978
  • Molecule weight243.11
  • Purity≥97%
  • MDL No.MFCD18383371

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

4-((4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)methyl)benzonitrile|CS-W021978

Structure of 475250-43-2

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General Information

  • CAS No. 475250-43-2
  • Cat. No. CS-W021978
  • Purity ≥97%
  • MDL No. MFCD18383371
  • Storage -20°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₄H₁₈BNO₂
  • Molecular Weight 243.11
  • Synonym(s) (4-CYANOBENZYL)BORONIC ACID PINACOL ESTER
  • SMILES N#CC1=CC=C(CB2OC(C)(C)C(C)(C)O2)C=C1

Description

4-((4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)methyl)benzonitrile features a boronate ester group flanked by a nitrile-substituted benzyl linker, enabling efficient Suzuki-Miyaura coupling under mild conditions. This bench-stable reagent integrates readily into complex molecular architectures with minimal functional group interference.

Application

4-((4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)methyl)benzonitrile serves as a robust boronate building block for Suzuki-Miyaura cross-coupling reactions. The nitrile group enables downstream functionalization via hydrolysis or reduction, while the stable, bench-ready boronate moiety facilitates efficient coupling with aryl halides and pseudohalides under mild conditions. Its compatibility with diverse functional groups and ease of purification make it a practical choice for constructing biaryl and heterocyclic scaffolds in medicinal chemistry and materials science.

Safety Information

Download SDS
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

Quality Control

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Computational Chemistry Data

  • TPSA   42.25
  • LogP   2.73218
  • H_Acceptors   3
  • H_Donors   0
  • Rotatable_Bonds   2

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