Description

6-Bromohexyl Acetate (CAS No. 68797-94-4) is a high-purity organic compound with the molecular formula C₈H₁₅BrO₂. This versatile brominated ester is widely utilized in organic synthesis, pharmaceutical research, and material science applications. The compound features a hexyl chain terminated by a bromine atom at the 6-position and an acetate group, making it a valuable intermediate for nucleophilic substitution reactions, polymer modifications, and cross-coupling methodologies.

Our 6-Bromohexyl Acetate is rigorously tested to ensure exceptional quality, with purity levels suitable for demanding research applications. It is supplied in sealed containers under inert atmosphere to maintain stability and prevent degradation. Proper storage conditions (2-8°C, dry environment) are recommended to preserve its reactivity and shelf life.

Key applications include use as a building block for:

• Functionalized polymer synthesis
• Pharmaceutical intermediates
• Liquid crystal materials
• Surface modification agents

Safety Data Sheets and Certificate of Analysis are available upon request. For research use only.

Properties

• CAS Number: 68797-94-4
• Complexity: 104
• IUPAC Name: 6-bromohexyl acetate
• InChI: InChI=1S/C8H15BrO2/c1-8(10)11-7-5-3-2-4-6-9/h2-7H2,1H3
• InChI Key: IMSPZLCTPSXORJ-UHFFFAOYSA-N
• Exact Mass: 222.02554
• Molecular Formula: C8H15BrO2
• Molecular Weight: 223.11
• SMILES: CC(=O)OCCCCCCBr
• Topological: 26.3
• Monoisotopic Mass: 222.02554
• Synonyms: 6-bromohexyl Acetate, 68797-94-4, DTXSID00473154, DTXCID10423968, 6-ACETOXY-1-BROMOHEXANE, SCHEMBL52919, neo-Clear(R)xylene substitute, MFCD02258467, AKOS015837795, AT35581, DB-253503

Application

6-Bromohexyl Acetate serves as a key intermediate in organic synthesis, particularly in the preparation of functionalized polymers through nucleophilic substitution reactions. Researchers utilize this compound in pharmaceutical development for creating prodrugs and bioactive molecules with extended alkyl chains. The bromine moiety enables efficient cross-coupling reactions in palladium-catalyzed transformations, while the acetate group provides a protected alcohol functionality for subsequent deprotection and derivatization.

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Disclaimer: Sold exclusively for laboratory research. Prohibited for commercial use, diagnostics, or human/animal applications. Buyers assume all compliance liability.