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CS-W001157 4
Total: USD 88.00

2-Bromo-4-chloropyrimidine

  • CAS No. 885702-33-0

  • Cat. No. CS-0042747
  • Purity≥95%
  • MDL No.MFCD11847634

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

2-Bromo-4-chloropyrimidine|CS-0042747

Structure of 885702-33-0

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General Information

  • CAS No. 885702-33-0
  • Cat. No. CS-0042747
  • Purity ≥95%
  • MDL No. MFCD11847634
  • Storage -20°C, sealed storage, away from moisture
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₄H₂BrClN₂
  • Molecular Weight 193.43
  • Synonym(s) Pyrimidine, 2-bromo-4-chloro- (9CI)
  • SMILES ClC1=NC(Br)=NC=C1

Description

2-Bromo-4-chloropyrimidine is a halogenated pyrimidine derivative featuring complementary reactive sites for cross-coupling and nucleophilic substitution. This bench-stable heterocycle integrates readily into medicinal chemistry scaffolds, enabling efficient access to functionalized pyrimidines under standard conditions.

Application

2-Bromo-4-chloropyrimidine serves as a versatile building block in heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions and nucleophilic substitution processes. Its orthogonal halogen reactivity facilitates selective functionalization at either the 2- or 4-position, supporting the construction of complex pyrimidine-based scaffolds. The compound exhibits excellent bench stability and ease of purification, making it well-suited for scalable medicinal chemistry campaigns and API intermediate development.

Synthesis

  • Route1

    References

    • Mosrin, Marc; Petrera, Marilena; Knochel, Paul Synthesis, 2008 , # 22 p. 3697 - 3702

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   25.78
  • LogP   1.8925
  • H_Acceptors   2
  • H_Donors   0
  • Rotatable_Bonds   0

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