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Structure of 223668-64-2
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Trimethoxy(pentafluorophenyl)silane features a pentafluorophenyl group attached to a silicon center bearing three methoxy groups. This combination delivers high reactivity in hydrosilylation and coupling reactions, with enhanced stability under standard conditions. The electron-deficient aromatic ring facilitates efficient cross-coupling processes, while the methoxy substituents enable controlled hydrolysis for surface functionalization.
Trimethoxy(pentafluorophenyl)silane serves as a robust silylating agent for hydroxyl and amine functionalities, enabling efficient protection and functional group manipulation. Its pentafluorophenyl moiety enhances leaving-group stability and reactivity in nucleophilic substitution, facilitating clean coupling reactions. The trimethoxy groups provide high solubility and stability under standard bench conditions, while the fluorinated aryl unit offers excellent functional group tolerance. This compound functions effectively in peptide synthesis, oligonucleotide modification, and polymer functionalization workflows.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H227-H315-H319
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Precautionary Statements : P210-P264-P280-P302+P352-P362+P364-P370+P378-P403-P501
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Lot numbers can be found on the outside label of a product: