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CS-W001157 4
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2-Bromo-N-methylpyridin-4-amine

  • CAS No. 847799-64-8

  • Cat. No. CS-0151032
  • Purity≥97%
  • MDL No.MFCD18259179

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

2-Bromo-N-methylpyridin-4-amine|CS-0151032

Structure of 847799-64-8

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General Information

  • CAS No. 847799-64-8
  • Cat. No. CS-0151032
  • Purity ≥97%
  • MDL No. MFCD18259179
  • Storage 4°C, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₆H₇BrN₂
  • Molecular Weight 187.04
  • Synonym(s) 2-Bromo-N-methyl-4-pyridinamine 847799-64-8
  • SMILES CNC1=CC(=NC=C1)Br

Description

2-Bromo-N-methylpyridin-4-amine features a bromine substituent at the pyridine ring’s 2-position and a methylamino group at the 4-position, enabling direct functionalization in cross-coupling reactions. The electron-deficient pyridine ring enhances reactivity toward palladium-catalyzed transformations, while the N-methyl group improves solubility and stability under standard conditions. This compound serves as a key building block for bioactive heterocycles in medicinal chemistry.

Application

2-Bromo-N-methylpyridin-4-amine serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions to access biologically relevant pyridine derivatives. Its bromo group facilitates efficient Suzuki, Stille, and Negishi couplings, while the N-methylpyridin-4-amine moiety provides a basic nitrogen for further functionalization or metal coordination. The compound exhibits good bench stability and is compatible with standard purification techniques, making it well-suited for iterative synthesis workflows in drug discovery.

Safety Information

Download SDS
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   24.92
  • LogP   1.8858
  • H_Acceptors   2
  • H_Donors   1
  • Rotatable_Bonds   1

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