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Methyl 1-methyl-4-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrole-2-carboxylate

  • CAS No. 1351379-23-1

  • Cat. No. CS-0177525
  • Molecule weight265.11
  • Purity≥95%
  • MDL No.None

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

Methyl 1-methyl-4-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrole-2-carboxylate|CS-0177525

Structure of 1351379-23-1

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General Information

  • CAS No. 1351379-23-1
  • Cat. No. CS-0177525
  • Purity ≥95%
  • MDL No. None
  • Storage -20°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₃H₂₀BNO₄
  • Molecular Weight 265.11
  • Synonym(s) None
  • SMILES O=C(C1=CC(B2OC(C)(C)C(C)(C)O2)=CN1C)OC

Description

Methyl 1-methyl-4-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrole-2-carboxylate features a boronate ester group integrated into a pyrrole scaffold, enabling efficient cross-coupling reactions. The tetramethyl-1,3,2-dioxaborolane moiety imparts enhanced stability and compatibility under standard reaction conditions. This bench-stable reagent streamlines the construction of complex heterocyclic architectures in synthetic organic chemistry and medicinal discovery.

Application

Methyl 1-methyl-4-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrole-2-carboxylate serves as a versatile boron building block for Suzuki-Miyaura cross-coupling reactions. The tetramethylboronate group enables efficient coupling with aryl and heteroaryl halides under mild conditions, while the pyrrole core provides a platform for constructing biologically relevant heterocyclic scaffolds. Bench-stable and compatible with diverse functional groups, it facilitates rapid access to complex molecular architectures in medicinal chemistry and materials science workflows.

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

Quality Control

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Computational Chemistry Data

  • TPSA   49.69
  • LogP   1.1109
  • H_Acceptors   5
  • H_Donors   0
  • Rotatable_Bonds   2

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