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CS-W001157 4
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5-Chloro-2-methylpyrimidin-4-amine

  • CAS No. 438249-95-7

  • Cat. No. CS-0045639
  • Purity≥97%
  • MDL No.None

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

5-Chloro-2-methylpyrimidin-4-amine|CS-0045639

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General Information

  • CAS No. 438249-95-7
  • Cat. No. CS-0045639
  • Purity ≥97%
  • MDL No. None
  • Storage 4°C, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₅H₆ClN₃
  • Molecular Weight 143.57
  • Synonym(s) 4-Pyrimidinamine, 5-chloro-2-methyl- (9CI)
  • SMILES NC1=NC(C)=NC=C1Cl

Description

5-Chloro-2-methylpyrimidin-4-amine serves as a key heterocyclic scaffold in medicinal chemistry, featuring a chlorinated pyrimidine core with a methyl group at the 2-position and a primary amine at C4. This configuration enables efficient coupling reactions and enhances metabolic stability in bioactive molecule design. The compound demonstrates excellent solubility under standard conditions and exhibits robust bench-stability, facilitating its use in multi-step synthetic sequences.

Application

5-Chloro-2-methylpyrimidin-4-amine serves as a versatile building block in medicinal chemistry, enabling efficient access to pyrimidine-based scaffolds through nucleophilic substitution and transition-metal-catalyzed coupling reactions. Its chlorine at C5 and amino group at C4 provide orthogonal reactivity for sequential functionalization, while the methyl group enhances metabolic stability. The compound exhibits excellent bench stability and facilitates straightforward purification, making it well-suited for high-throughput synthesis and API development workflows.

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   51.8
  • LogP   1.02062
  • H_Acceptors   3
  • H_Donors   1
  • Rotatable_Bonds   0

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