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Atomfair Heptadecan-9-yl 8-bromooctanoate C25H49BrO2
Description Heptadecan-9-yl 8-bromooctanoate (CAS No. 2089253-22-3) is a high-purity brominated ester compound with the molecular formula C25H49BrO2. This specialized chemical is designed for advanced research and industrial applications, offering exceptional stability and reactivity due to its unique aliphatic bromine-functionalized structure. With a molecular weight of 461.56 g/mol, it is supplied as a clear to pale-yellow liquid or low-melting solid, ensuring ease of handling in synthetic workflows. Ideal for organic synthesis, material science, and pharmaceutical research, this compound is rigorously tested for purity (typically ??95% by HPLC or GC analysis) and consistency. Store under inert conditions at recommended temperatures to maintain…
Description
Description
Heptadecan-9-yl 8-bromooctanoate (CAS No. 2089253-22-3) is a high-purity brominated ester compound with the molecular formula C25H49BrO2. This specialized chemical is designed for advanced research and industrial applications, offering exceptional stability and reactivity due to its unique aliphatic bromine-functionalized structure. With a molecular weight of 461.56 g/mol, it is supplied as a clear to pale-yellow liquid or low-melting solid, ensuring ease of handling in synthetic workflows. Ideal for organic synthesis, material science, and pharmaceutical research, this compound is rigorously tested for purity (typically ??95% by HPLC or GC analysis) and consistency. Store under inert conditions at recommended temperatures to maintain optimal stability.
- CAS No: 2089253-22-3
- Molecular Formula: C25H49BrO2
- Molecular Weight: 461.6
- Exact Mass: 460.29159
- Monoisotopic Mass: 460.29159
- IUPAC Name: heptadecan-9-yl 8-bromooctanoate
- SMILES: CCCCCCCCC(CCCCCCCC)OC(=O)CCCCCCCBr
- Synonyms: heptadecan-9-yl 8-bromooctanoate, 2089253-22-3, 870-767-1, 9-Heptadecyl 8-Bromooctanoate, SCHEMBL18641748
Application
Heptadecan-9-yl 8-bromooctanoate serves as a versatile intermediate in organic synthesis, particularly for introducing bromoalkyl chains into target molecules. Researchers utilize it in polymer modification to enhance flame retardancy or as a precursor for phase-transfer catalysts. Its amphiphilic structure also makes it valuable in surfactant studies and nanotechnology applications requiring controlled self-assembly.
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