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CS-W001157 4
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5-Bromo-2-chloro-3-nitropyridin-4-amine

  • CAS No. 1334136-60-5

  • Cat. No. CS-0035823
  • Purity≥98%
  • MDL No.None

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

5-Bromo-2-chloro-3-nitropyridin-4-amine|CS-0035823

Structure of 1334136-60-5

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General Information

  • CAS No. 1334136-60-5
  • Cat. No. CS-0035823
  • Purity ≥98%
  • MDL No. None
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₅H₃BrClN₃O₂
  • Molecular Weight 252.45
  • Synonym(s) 2-broMo-5-chloro-3-nitropyridin-4-aMine
  • SMILES C1=C(C(=C(C(=N1)Cl)[N+](=O)[O-])N)Br

Description

5-Bromo-2-chloro-3-nitropyridin-4-amine features a pyridine core functionalized with bromo, chloro, and nitro groups at strategic positions, enabling direct incorporation into cross-coupling and cyclization workflows. The electron-deficient aromatic framework supports efficient metal-catalyzed transformations, while the amine handle facilitates downstream derivatization in medicinal chemistry and materials synthesis.

Application

5-Bromo-2-chloro-3-nitropyridin-4-amine serves as a versatile building block in heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions due to its compatible halogen functionalities. The nitro group facilitates selective reductions and further functionalization, while the amino handle allows for derivatization via acylation or coupling. Its bench-stable nature and orthogonal reactivity profile support efficient, multi-step synthetic sequences in medicinal chemistry and agrochemical development.

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-H311-H331
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P361-P405-P501

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Computational Chemistry Data

  • TPSA   82.05
  • LogP   1.9879
  • H_Acceptors   4
  • H_Donors   1
  • Rotatable_Bonds   1

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