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CS-W001157 4
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6-Bromo-4-fluoro-2-methylbenzo[d]thiazole

  • CAS No. 1427433-65-5

  • Cat. No. CS-0527235
  • Molecule weight246.10
  • Purity≥98%
  • MDL No.None

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

6-Bromo-4-fluoro-2-methylbenzo[d]thiazole|CS-0527235

Structure of 1427433-65-5

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General Information

  • CAS No. 1427433-65-5
  • Cat. No. CS-0527235
  • Purity ≥98%
  • MDL No. None
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₈H₅BrFNS
  • Molecular Weight 246.10
  • Synonym(s) 6-Bromo-4-fluoro-2-methyl-1,3-benzothiazole
  • SMILES CC1=NC2=C(F)C=C(Br)C=C2S1

Description

6-Bromo-4-fluoro-2-methylbenzo[d]thiazole features a fused heterocyclic core with strategically positioned halogen and methyl substituents. This electron-deficient scaffold enables efficient coupling in cross-coupling reactions, particularly Pd-catalyzed variants. The bromine atom serves as a high-reactivity handle for C–C bond formation, while the fluorine enhances metabolic stability and modulates electronic properties. Bench-stable under standard conditions, it integrates readily into complex molecular architectures.

Application

6-Bromo-4-fluoro-2-methylbenzo[d]thiazole serves as a versatile building block in the synthesis of biologically active heterocycles and pharmaceutical intermediates. Its orthogonal halogenation pattern enables selective cross-coupling reactions, while the methyl group provides a handle for further functionalization. The molecule exhibits excellent bench stability and compatibility with palladium-catalyzed transformations, facilitating efficient access to complex scaffolds in medicinal chemistry and process development workflows.

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-P405-P501

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Computational Chemistry Data

  • TPSA   12.89
  • LogP   3.50632
  • H_Acceptors   2
  • H_Donors   0
  • Rotatable_Bonds   0

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