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Structure of 17201-83-1
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This chloromethyl-functionalized disiloxane delivers a highly reactive electrophilic handle for silicon-directed conjugation. The pentamethyl-substituted framework imparts exceptional steric shielding and moisture tolerance, enabling reliable coupling under standard bench conditions.
1-(Chloromethyl)-1,1,3,3,3-pentamethyldisiloxane serves as a robust, bench-stable silyl-protecting group reagent that enables selective functionalization of nucleophiles under mild conditions. Its sterically shielded disiloxane backbone enhances stability and minimizes side reactions, while the chloromethyl group facilitates efficient alkylation and downstream transformations. Ideal for constructing complex architectures in medicinal chemistry and materials science workflows.
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GHS Pictogram :
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GHS No : GHS02,GHS07
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Signal Word : Danger
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UN#: 1993
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Class : 3
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Packing Group : Ⅲ
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Hazard Statements : H225-H315-H319-H335
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Precautionary Statements : P210-P233-P240-P241-P242-P243-P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P370+P378-P405-P501
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Lot numbers can be found on the outside label of a product: