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CS-W001157 4
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4-Bromo-5-methylpicolinaldehyde

  • CAS No. 1196157-14-8

  • Cat. No. CS-W022111
  • Purity≥98%
  • MDL No.MFCD13190304

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

4-Bromo-5-methylpicolinaldehyde|CS-W022111

Structure of 1196157-14-8

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General Information

  • CAS No. 1196157-14-8
  • Cat. No. CS-W022111
  • Purity ≥98%
  • MDL No. MFCD13190304
  • Storage -20°C, sealed storage, away from moisture
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₇H₆BrNO
  • Molecular Weight 200.03
  • Synonym(s) None
  • SMILES O=CC1=NC=C(C)C(Br)=C1

Description

4-Bromo-5-methylpicolinaldehyde features a brominated pyridine core with a methyl substituent and aldehyde functionality, enabling direct incorporation into cross-coupling reactions. The electron-deficient heteroaryl ring facilitates palladium-catalyzed transformations, while the aldehyde group offers downstream derivatization potential. This bench-stable reagent streamlines access to complex nitrogen-containing scaffolds in medicinal chemistry and materials synthesis.

Application

4-Bromo-5-methylpicolinaldehyde serves as a versatile building block in medicinal chemistry and cross-coupling synthesis. Its aldehyde functionality enables direct incorporation into imines, oximes, and reductive amination workflows, while the bromine atom facilitates palladium-catalyzed coupling reactions. The methyl group enhances lipophilicity and provides a handle for further functionalization. This compound exhibits good bench stability and is compatible with standard reaction conditions, making it suitable for iterative synthetic sequences in API development.

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   29.96
  • LogP   1.96502
  • H_Acceptors   2
  • H_Donors   0
  • Rotatable_Bonds   1

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