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CS-W001157 4
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2-Amino-5-bromonicotinaldehyde

  • CAS No. 206997-15-1

  • Cat. No. CS-0042672
  • Purity≥98%
  • MDL No.MFCD09607904

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

2-Amino-5-bromonicotinaldehyde|CS-0042672

Structure of 206997-15-1

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General Information

  • CAS No. 206997-15-1
  • Cat. No. CS-0042672
  • Purity ≥98%
  • MDL No. MFCD09607904
  • Storage 4°C, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₆H₅BrN₂O
  • Molecular Weight 201.02
  • Synonym(s) 2-amino-5-bromopyridine-3-carbaldehyde
  • SMILES O=CC1=C(N)N=CC(Br)=C1

Description

2-Amino-5-bromonicotinaldehyde features a brominated pyridine core with complementary amino and aldehyde functionalities, enabling direct coupling in cross-coupling and condensation reactions. This bench-stable reagent integrates readily into synthetic pathways requiring electron-deficient heterocyclic scaffolds.

Application

2-Amino-5-bromonicotinaldehyde serves as a versatile building block in medicinal chemistry, enabling the synthesis of heterocyclic scaffolds via condensation and coupling reactions. Its amino and aldehyde functionalities offer orthogonal reactivity for diverse transformations, while the bromine substituent facilitates palladium-catalyzed cross-coupling. The compound exhibits good bench stability and is readily purified by crystallization, supporting efficient integration into multi-step synthetic sequences.

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   55.98
  • LogP   1.2388
  • H_Acceptors   3
  • H_Donors   1
  • Rotatable_Bonds   1

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