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CS-W001157 4
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2-Bromo-5-chlorobenzo[d]thiazole

  • CAS No. 2941-56-2

  • Cat. No. CS-0103346
  • Purity≥97%
  • MDL No.MFCD09749223

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

2-Bromo-5-chlorobenzo[d]thiazole|CS-0103346

Structure of 2941-56-2

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General Information

  • CAS No. 2941-56-2
  • Cat. No. CS-0103346
  • Purity ≥97%
  • MDL No. MFCD09749223
  • Storage 4°C, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₇H₃BrClNS
  • Molecular Weight 248.53
  • Synonym(s) 4,9-DIMETHYLCYCLOHEXYLAMINEHYDROCHLORIDE
  • SMILES ClC1=CC=C2SC(Br)=NC2=C1

Description

2-Bromo-5-chlorobenzo[d]thiazole features a fused heterocyclic core bearing bromo and chloro substituents at electron-rich positions, enabling direct functionalization in cross-coupling reactions. The strategic placement of halogens facilitates palladium-catalyzed transformations, while the rigid aromatic system enhances metabolic stability and binding affinity in medicinal chemistry applications. This compound serves as a key scaffold for synthesizing bioactive molecules and advanced materials.

Application

2-Bromo-5-chlorobenzo[d]thiazole serves as a versatile building block in medicinal chemistry and materials science, enabling palladium-catalyzed cross-coupling reactions due to its orthogonal halogen reactivity. The bromine site facilitates efficient Suzuki, Stille, or Negishi coupling, while the chlorine offers stability under standard reaction conditions. Its bench-stable crystalline form simplifies handling and purification, making it well-suited for modular synthesis of complex heterocyclic scaffolds and functionalized aromatic systems.

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

Quality Control

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Computational Chemistry Data

  • TPSA   12.89
  • LogP   3.7122
  • H_Acceptors   2
  • H_Donors   0
  • Rotatable_Bonds   0

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