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CS-W001157 4
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5-Bromo-2-chloroisonicotinaldehyde

  • CAS No. 1060802-23-4

  • Cat. No. CS-0039821
  • Purity≥96%
  • MDL No.MFCD11847346

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

5-Bromo-2-chloroisonicotinaldehyde|CS-0039821

Structure of 1060802-23-4

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General Information

  • CAS No. 1060802-23-4
  • Cat. No. CS-0039821
  • Purity ≥96%
  • MDL No. MFCD11847346
  • Storage -20°C, stored under nitrogen
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₆H₃BrClNO
  • Molecular Weight 220.45
  • Synonym(s) 5-Bromo-2-Chloropyridine-4-Carboxaldehyde
  • SMILES O=CC1=CC(Cl)=NC=C1Br

Description

5-Bromo-2-chloroisonicotinaldehyde features a highly reactive aldehyde group flanked by bromo and chloro substituents at the 5- and 2-positions of the pyridine ring. This electron-deficient scaffold enables direct incorporation into cross-coupling reactions, offering precise control over regiochemistry in synthetic sequences. The compound demonstrates stability under standard handling conditions and serves as a key building block for functionalized heterocycles.

Application

5-Bromo-2-chloroisonicotinaldehyde serves as a versatile building block in medicinal chemistry, enabling direct incorporation of halogenated pyridine motifs into target molecules. Its aldehyde functionality facilitates nucleophilic addition and condensation reactions, while the ortho-halogen substituents support palladium-catalyzed cross-coupling transformations. The compound exhibits good bench stability and is compatible with standard protecting group strategies, making it well-suited for modular synthesis of functionalized heterocycles and API intermediates.

Safety Information

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GHS Pictogram :
GHS No : GHS06
Signal Word : Danger
UN#: 2811
Class : 6.1
Packing Group : Ⅲ
Hazard Statements : H301-H315-H319-H335
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362-P405-P501

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Computational Chemistry Data

  • TPSA   29.96
  • LogP   2.31
  • H_Acceptors   2
  • H_Donors   0
  • Rotatable_Bonds   1

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