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Methyl 3-bromo-1H-pyrrolo[3,2-b]pyridine-5-carboxylate

  • CAS No. 1190318-72-9

  • Cat. No. CS-0054455
  • Purity≥98%
  • MDL No.None

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

Methyl 3-bromo-1H-pyrrolo[3,2-b]pyridine-5-carboxylate|CS-0054455

Structure of 1190318-72-9

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General Information

  • CAS No. 1190318-72-9
  • Cat. No. CS-0054455
  • Purity ≥98%
  • MDL No. None
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₉H₇BrN₂O₂
  • Molecular Weight 255.07
  • Synonym(s) 3-BroMo-4-azaindole-5-carboxylic acid Methyl ester
  • SMILES O=C(C1=CC=C2NC=C(Br)C2=N1)OC

Description

Methyl 3-bromo-1H-pyrrolo[3,2-b]pyridine-5-carboxylate features a brominated pyrrolopyridine core with a methyl ester at the C5 position, enabling direct functionalization in cross-coupling reactions. The electron-deficient heterocycle facilitates palladium-catalyzed transformations, while the bench-stable ester group supports straightforward derivatization under standard conditions.

Application

Methyl 3-bromo-1H-pyrrolo[3,2-b]pyridine-5-carboxylate serves as a versatile building block for the synthesis of functionalized heterocycles and bioactive scaffolds. The bromo group enables palladium-catalyzed cross-coupling reactions, while the ester functionality supports further derivatization via hydrolysis or nucleophilic substitution. Its bench-stable nature and compatibility with standard reaction conditions facilitate efficient integration into medicinal chemistry and process development 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

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Computational Chemistry Data

  • TPSA   54.98
  • LogP   2.112
  • H_Acceptors   3
  • H_Donors   1
  • Rotatable_Bonds   1

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