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Atomfair (Chloromethyl)bis(4-fluorophenyl)methylsilane C14H13ClF2Si
Description (Chloromethyl)bis(4-fluorophenyl)methylsilane (CAS No. 85491-26-5) is a high-purity organosilane compound with the molecular formula C14H13ClF2Si . This specialized chemical features a chloromethyl group and bis(4-fluorophenyl)methyl substituents bonded to a central silicon atom, making it a valuable intermediate in organic synthesis and materials science. Its unique structure enables applications in pharmaceuticals, agrochemicals, and advanced polymer systems. Our product is rigorously tested to ensure ??95% purity (GC), with moisture and impurity levels minimized for optimal performance. Available in amber glass bottles under inert gas to preserve stability. Suitable for researchers requiring precise functionalization of silicon-based compounds.
Description
Description
(Chloromethyl)bis(4-fluorophenyl)methylsilane (CAS No. 85491-26-5) is a high-purity organosilane compound with the molecular formula C14H13ClF2Si. This specialized chemical features a chloromethyl group and bis(4-fluorophenyl)methyl substituents bonded to a central silicon atom, making it a valuable intermediate in organic synthesis and materials science. Its unique structure enables applications in pharmaceuticals, agrochemicals, and advanced polymer systems. Our product is rigorously tested to ensure ??95% purity (GC), with moisture and impurity levels minimized for optimal performance. Available in amber glass bottles under inert gas to preserve stability. Suitable for researchers requiring precise functionalization of silicon-based compounds.
- CAS No: 85491-26-5
- Molecular Formula: C14H13ClF2Si
- Molecular Weight: 282.79
- Exact Mass: 282.0443110
- Monoisotopic Mass: 282.0443110
- IUPAC Name: bis(4-fluorophenyl)methyl-(chloromethyl)silane
- SMILES: C1=CC(=CC=C1C(C2=CC=C(C=C2)F)[SiH2]CCl)F
- Synonyms: (Chloromethyl)bis(4-fluorophenyl)methylsilane, 85491-26-5, EC 401-200-4, 401-200-4, bis(4-fluorophenyl)methyl-(chloromethyl)silane
Application
This organosilane serves as a key building block for synthesizing fluorinated silicon-containing compounds in medicinal chemistry. The reactive chloromethyl group enables further functionalization for drug discovery applications. It’s also used in surface modification of silica materials and as a precursor for specialty silicones with enhanced thermal stability. The fluorophenyl groups contribute to lipophilicity in designed molecules.
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