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CS-W001157 4
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5-Bromo-6-methoxy-1H-pyrrolo[2,3-b]pyridine

  • CAS No. 1190321-63-1

  • Cat. No. CS-0041904
  • Purity≥97%
  • MDL No.None

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

5-Bromo-6-methoxy-1H-pyrrolo[2,3-b]pyridine|CS-0041904

Structure of 1190321-63-1

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General Information

  • CAS No. 1190321-63-1
  • Cat. No. CS-0041904
  • Purity ≥97%
  • MDL No. None
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₈H₇BrN₂O
  • Molecular Weight 227.06
  • Synonym(s) 5-Bromo-6-methoxy-7-zazindole
  • SMILES COC1=C(Br)C=C2C(NC=C2)=N1

Description

5-Bromo-6-methoxy-1H-pyrrolo[2,3-b]pyridine is a heteroaromatic building block featuring a bromine at the 5-position and a methoxy group at the 6-position. This electron-deficient scaffold enables direct functionalization in cross-coupling reactions. The molecule exhibits robust stability under standard conditions and integrates readily into complex molecular architectures for medicinal chemistry and materials applications.

Application

5-Bromo-6-methoxy-1H-pyrrolo[2,3-b]pyridine serves as a versatile heterocyclic building block for C–H functionalization and cross-coupling reactions. The bromo group enables palladium-catalyzed coupling with diverse nucleophiles, while the methoxy substituent provides moderate electron donation and enhances solubility. Bench-stable and readily purified by column chromatography, it functions effectively in the synthesis of pharmaceutical scaffolds and agrochemical intermediates under standard reaction conditions.

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   37.91
  • LogP   2.334
  • H_Acceptors   2
  • H_Donors   1
  • Rotatable_Bonds   1

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