Atomfair 4-Bromo-2-(tributylstannyl)-1,3-thiazole C15H28BrNSSn

Description 4-Bromo-2-(tributylstannyl)-1,3-thiazole (CAS No. 173978-98-8) is a high-purity organotin compound with the molecular formula C15H28BrNSSn . This specialized reagent is widely used in organic synthesis, particularly in Stille coupling reactions, due to its reactivity as a stannyl-thiazole derivative. The compound features a bromo-substituted thiazole ring coupled with a tributylstannyl group, making it a versatile intermediate for constructing complex heterocyclic systems. Our product is rigorously tested to ensure exceptional quality, with detailed analytical data (NMR, HPLC, etc.) available upon request. Suitable for research and industrial applications, it is supplied in sealed containers under inert atmosphere to guarantee stability and longevity.

Description

Description

4-Bromo-2-(tributylstannyl)-1,3-thiazole (CAS No. 173978-98-8) is a high-purity organotin compound with the molecular formula C15H28BrNSSn. This specialized reagent is widely used in organic synthesis, particularly in Stille coupling reactions, due to its reactivity as a stannyl-thiazole derivative. The compound features a bromo-substituted thiazole ring coupled with a tributylstannyl group, making it a versatile intermediate for constructing complex heterocyclic systems. Our product is rigorously tested to ensure exceptional quality, with detailed analytical data (NMR, HPLC, etc.) available upon request. Suitable for research and industrial applications, it is supplied in sealed containers under inert atmosphere to guarantee stability and longevity.

  • CAS No: 173978-98-8
  • Molecular Formula: C15H28BrNSSn
  • Molecular Weight: 453.1
  • Exact Mass: 453.01479
  • Monoisotopic Mass: 453.01479
  • IUPAC Name: (4-bromo-1,3-thiazol-2-yl)-tributylstannane
  • SMILES: CCCC[Sn](CCCC)(CCCC)C1=NC(=CS1)Br
  • Synonyms: 4-Bromo-2-(tributylstannyl)-1,3-thiazole, 630-660-0, 4-Bromo-2-(tributylstannyl)thiazole, 173978-98-8, Thiazole, 4-bromo-2-(tributylstannyl)-

Application

4-Bromo-2-(tributylstannyl)-1,3-thiazole is primarily employed in Stille cross-coupling reactions to form C-C bonds in pharmaceutical and materials science research. It serves as a key building block for synthesizing functionalized thiazole derivatives, which are prevalent in bioactive molecules. The compound is also used in the development of organic electronic materials due to its ability to introduce thiazole motifs into conjugated systems.

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