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3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-5,6-dihydro-4H-pyrrolo[1,2-b]pyrazole

  • CAS No. 1314138-13-0

  • Cat. No. CS-0042508
  • Purity≥97%
  • MDL No.None

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

3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-5,6-dihydro-4H-pyrrolo[1,2-b]pyrazole|CS-0042508

Structure of 1314138-13-0

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General Information

  • CAS No. 1314138-13-0
  • Cat. No. CS-0042508
  • Purity ≥97%
  • MDL No. None
  • Storage -20°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₂H₁₉BN₂O₂
  • Molecular Weight 234.10
  • Synonym(s) 5,6-dihydro-4H-pyrrolo[1,2-b]pyrazole-3-boronic acid pinacol ester
  • SMILES CC1(C)C(C)(C)OB(C2=C(CCC3)N3N=C2)O1

Description

This boronate-functionalized pyrrolopyrazole integrates readily into Suzuki-Miyaura coupling reactions under standard conditions. The tetramethylborolane moiety ensures high stability and compatibility with diverse reaction environments, enabling efficient C–C bond formation in complex molecular architectures.

Application

3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-5,6-dihydro-4H-pyrrolo[1,2-b]pyrazole serves as a versatile boron-containing building block for Suzuki-Miyaura cross-coupling reactions. Its stable dioxaborolane group enables efficient C–C bond formation under mild conditions, while the dihydropyrrolopyrazole core provides a rigid, nitrogen-rich heterocyclic scaffold relevant to medicinal chemistry and functional materials. The compound exhibits excellent bench stability, minimal air sensitivity, and compatibility with diverse functional groups, facilitating straightforward purification and integration into complex molecular architectures.

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-P330-P362+P364-P405-P501

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Computational Chemistry Data

  • TPSA   36.28
  • LogP   1.1285
  • H_Acceptors   4
  • H_Donors   0
  • Rotatable_Bonds   1

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