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CS-W001157 4
Total: USD 88.00

6-Chloro-3-iodo-1H-pyrrolo[3,2-c]pyridine

  • CAS No. 1000341-55-8

  • Cat. No. CS-0041201
  • Purity≥95%
  • MDL No.None

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

6-Chloro-3-iodo-1H-pyrrolo[3,2-c]pyridine|CS-0041201

Structure of 1000341-55-8

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General Information

  • CAS No. 1000341-55-8
  • Cat. No. CS-0041201
  • Purity ≥95%
  • MDL No. None
  • Storage 4°C, protect from light, stored under nitrogen
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₇H₄ClIN₂
  • Molecular Weight 278.48
  • Synonym(s) 6-Chloro-3-iodo-5-azaindole
  • SMILES IC1=CNC2=C1C=NC(Cl)=C2

Description

6-Chloro-3-iodo-1H-pyrrolo[3,2-c]pyridine is a halogenated heterocyclic scaffold featuring complementary reactive sites for cross-coupling transformations. The electron-deficient pyrrolopyridine core enables efficient palladium-catalyzed functionalization, while the chloro and iodo substituents offer orthogonal reactivity. This molecule serves as a key building block in the synthesis of complex nitrogen-containing architectures relevant to medicinal chemistry and materials science.

Application

6-Chloro-3-iodo-1H-pyrrolo[3,2-c]pyridine serves as a versatile building block for constructing biologically relevant heterocyclic scaffolds. The orthogonal reactivity of the chloro and iodo groups enables sequential cross-coupling reactions, facilitating efficient diversification in medicinal chemistry campaigns. Bench-stable and compatible with standard Pd-catalyzed transformations, it functions reliably in Suzuki, Stille, and Negishi coupling protocols, offering predictable regioselectivity and high functional group tolerance.

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   28.68
  • LogP   2.8209
  • H_Acceptors   1
  • H_Donors   1
  • Rotatable_Bonds   0

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