Description

2-(6-Chlorohexyloxy)tetrahydro-2H-pyran (CAS No. 2009-84-9) is a high-purity organic compound with the molecular formula C₁₁H₂₁ClO₂, widely used in synthetic chemistry and pharmaceutical research. This versatile intermediate features a chlorohexyloxy group tethered to a tetrahydro-2H-pyran (oxane) ring, making it ideal for nucleophilic substitution reactions, polymer modifications, and as a building block for complex molecular architectures. Its stability under inert conditions and compatibility with common organic solvents (e.g., THF, DCM) ensure reliable performance in lab-scale and industrial applications. Each batch is rigorously analyzed by GC/MS, NMR, and HPLC to guarantee ≥95% purity, with trace moisture and residual solvents minimized for sensitive reactions. Available in amber glass bottles or custom bulk packaging under nitrogen atmosphere to preserve integrity.

Properties

• CAS Number: 2009-84-9
• Complexity: 130
• IUPAC Name: 2-(6-chlorohexoxy)tetrahydropyran
• InChI: InChI=1S/C11H21ClO2/c12-8-4-1-2-5-9-13-11-7-3-6-10-14-11/h11H,1-10H2
• InChI Key: XOLOZSPDGPUSFV-UHFFFAOYSA-N
• Exact Mass: 220.1230076
• Molecular Formula: C11H21ClO2
• Molecular Weight: 220.73
• SMILES: C1CCOC(C1)OCCCCCCCl
• Topological: 18.5
• Monoisotopic Mass: 220.1230076
• Synonyms: 2009-84-9, 2-(6-Chlorohexyloxy)tetrahydro-2H-pyran, DTXSID60317323, DTXCID00268446, 2-(6-chlorohexoxy)oxane, 2-((6-Chlorohexyl)oxy)tetrahydro-2H-pyran, 2H-Pyran, 2-[(6-chlorohexyl)oxy]tetrahydro-, 2-[(6-CHLOROHEXYL)OXY]OXANE, NSC314555, 2-(6-Chlorohexyloxy)tetrahydro-2H-pyran&, SCHEMBL738953, 2-(6-chlorohexyloxy)tetrahydropyran, 2-(6-chlorohexyloxy)tetrahydropyrane, 2-(6-chloro-hexyloxy)tetrahydropyran, AKOS015912548, 2-(6-Chloro-hexyloxy)-tetrahydropyran, NSC-314555, 2-(6-Chloro-hexyloxy)-tetrahydro-pyran, 2-(6-chloro-1-hexyloxy)tetrahydropyrane, 2-[(6-Chlorohexyl)oxy]tetrahydro-2H-pyran #, F71616, 2-(6-Chlorohexyloxy)tetrahydro-2H-pyran, 95%

Application

2-(6-Chlorohexyloxy)tetrahydro-2H-pyran serves as a key intermediate in the synthesis of functionalized polymers and dendrimers, where its reactive chloro group enables controlled chain elongation. Researchers utilize it to develop drug-delivery systems by conjugating bioactive molecules via ether linkages. In materials science, it acts as a crosslinking agent for hydrophobic coatings and elastomers.

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