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Atomfair 2-(4-Bromobutoxy)tetrahydro-2H-pyran C9H17BrO2

Description 2-(4-Bromobutoxy)tetrahydro-2H-pyran (CAS No. 3181-38-2) is a high-purity brominated ether compound with the molecular formula C9H17BrO2, widely utilized in organic synthesis and pharmaceutical research. This specialized chemical features a tetrahydropyran (THP) group linked to a 4-bromobutoxy chain, offering versatile reactivity for nucleophilic substitutions and protective group strategies. Our product is rigorously tested via GC/HPLC to ensure ??98% purity, packaged under inert gas to prevent degradation, and supplied in amber glass vials for optimal stability. Ideal for constructing complex molecular architectures, it serves as a key intermediate in medicinal chemistry, agrochemical development, and materials science applications requiring precise bromoalkylation.

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Description

Description

2-(4-Bromobutoxy)tetrahydro-2H-pyran (CAS No. 3181-38-2) is a high-purity brominated ether compound with the molecular formula C9H17BrO2, widely utilized in organic synthesis and pharmaceutical research. This specialized chemical features a tetrahydropyran (THP) group linked to a 4-bromobutoxy chain, offering versatile reactivity for nucleophilic substitutions and protective group strategies. Our product is rigorously tested via GC/HPLC to ensure ??98% purity, packaged under inert gas to prevent degradation, and supplied in amber glass vials for optimal stability. Ideal for constructing complex molecular architectures, it serves as a key intermediate in medicinal chemistry, agrochemical development, and materials science applications requiring precise bromoalkylation.

  • CAS No: 3181-38-2
  • Molecular Formula: C9H17BrO2
  • Molecular Weight: 237.13
  • Exact Mass: 236.04119
  • Monoisotopic Mass: 236.04119
  • IUPAC Name: 2-(4-bromobutoxy)oxane
  • SMILES: C1CCOC(C1)OCCCCBr
  • Synonyms: 2-(4-Bromobutoxy)tetrahydro-2H-pyran, 31608-22-7, DTXSID00339827, DTXCID40290908, 2-(4-bromobutoxy)oxane

Application

This compound is primarily employed as a bifunctional alkylating agent in heterocyclic synthesis, enabling the introduction of both THP-protected alcohols and bromoalkyl chains in single-step reactions. Researchers utilize it in Suzuki-Miyaura cross-coupling reactions to create extended carbon frameworks with oxygen-containing heterocycles. The THP group provides temporary hydroxyl protection during multi-step syntheses of bioactive molecules, particularly in nucleoside and prostaglandin analog development.

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