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CS-W001157 4
Total: USD 88.00

2-Bromo-5-iodopyridin-4-amine

  • CAS No. 1300750-78-0

  • Cat. No. CS-0444329
  • Purity≥97%
  • MDL No.MFCD27959281

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

2-Bromo-5-iodopyridin-4-amine|CS-0444329

Structure of 1300750-78-0

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General Information

  • CAS No. 1300750-78-0
  • Cat. No. CS-0444329
  • Purity ≥97%
  • MDL No. MFCD27959281
  • Storage 4°C, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₅H₄BrIN₂
  • Molecular Weight 298.91
  • Synonym(s) 4-amino-2-bromo-5-iodopyridine
  • SMILES C1=C(C(=CN=C1Br)I)N

Description

2-Bromo-5-iodopyridin-4-amine delivers a dual halogenation pattern on a pyridine scaffold, enabling efficient cross-coupling strategies in medicinal chemistry. The bromo and iodo groups facilitate sequential Pd-catalyzed transformations, while the primary amine supports direct derivatization or conjugation. This bifunctional reactivity profile supports rapid diversification of heterocyclic architectures in target-oriented synthesis.

Application

2-Bromo-5-iodopyridin-4-amine serves as a versatile building block in cross-coupling chemistry, enabling efficient access to substituted pyridine scaffolds. Its dual halogen functionality supports sequential or orthogonal coupling reactions, facilitating the construction of complex heterocyclic systems. The amine group provides additional handle for derivatization, while the compound exhibits good bench stability and compatibility with standard Pd-catalyzed transformations.

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-P330-P362+P364-P405-P501

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Computational Chemistry Data

  • TPSA   38.91
  • LogP   2.0309
  • H_Acceptors   2
  • H_Donors   1
  • Rotatable_Bonds   0

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