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CS-W001157 4
Total: USD 88.00

4-Bromo-2-methylbenzo[d]thiazole

  • CAS No. 112146-10-8

  • Cat. No. CS-0005532
  • Purity≥98%
  • MDL No.MFCD11217352

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

4-Bromo-2-methylbenzo[d]thiazole|CS-0005532

Structure of 112146-10-8

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General Information

  • CAS No. 112146-10-8
  • Cat. No. CS-0005532
  • Purity ≥98%
  • MDL No. MFCD11217352
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₈H₆BrNS
  • Molecular Weight 228.11
  • Synonym(s) 4-BROMO-2-METHYLBENZOTHIAZOLE
  • SMILES CC1=NC2=C(Br)C=CC=C2S1

Description

4-Bromo-2-methylbenzo[d]thiazole features a bromine substituent at the 4-position and a methyl group at the 2-position on a benzo[d]thiazole core. This electron-deficient heterocycle integrates readily into transition metal-catalyzed cross-coupling reactions, enabling efficient access to complex thiazole-based scaffolds under standard conditions.

Application

4-Bromo-2-methylbenzo[d]thiazole serves as a versatile building block in medicinal chemistry and materials science, enabling palladium-catalyzed cross-coupling reactions due to its well-defined halogen reactivity. The methyl group enhances electronic modulation and provides steric control in subsequent transformations. Its bench-stable nature and compatibility with standard synthetic protocols make it ideal for constructing complex heterocyclic scaffolds and functionalized aryl derivatives in high-throughput synthesis.

Synthesis

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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501

Quality Control

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Computational Chemistry Data

  • TPSA   12.89
  • LogP   3.36722
  • H_Acceptors   2
  • H_Donors   0
  • Rotatable_Bonds   0

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