Benzyl(chloromethyl)dimethylsilane

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Reagent Code: #129707
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CAS Number 5356-99-0

science Other reagents with same CAS 5356-99-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 198.76 g/mol
Formula C₁₀H₁₅ClSi
badge Registry Numbers
MDL Number MFCD01863486
thermostat Physical Properties
Boiling Point 120-124 °C at 40 mmHg(lit.)
inventory_2 Storage & Handling
Density 1.01 g/cm3 at 25 °C(lit.)
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used primarily as a silylating agent in organic synthesis, this compound serves to introduce the benzyl(dimethyl)silyl protecting group, particularly for alcohols and phenols. Its reactivity allows selective protection in complex molecule assembly, enhancing stability during multi-step reactions. The chloromethyl functionality enables further derivatization through nucleophilic substitution, making it valuable in the design of pharmaceutical intermediates and functionalized silanes for materials science. It is also employed in the preparation of crosslinking agents for silicon-based polymers, contributing to improved thermal and mechanical properties in cured resins.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿10,080.00
inventory 1g
10-20 days ฿27,180.00

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Benzyl(chloromethyl)dimethylsilane
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Used primarily as a silylating agent in organic synthesis, this compound serves to introduce the benzyl(dimethyl)silyl protecting group, particularly for alcohols and phenols. Its reactivity allows selective protection in complex molecule assembly, enhancing stability during multi-step reactions. The chloromethyl functionality enables further derivatization through nucleophilic substitution, making it valuable in the design of pharmaceutical intermediates and functionalized silanes for materials science.

Used primarily as a silylating agent in organic synthesis, this compound serves to introduce the benzyl(dimethyl)silyl protecting group, particularly for alcohols and phenols. Its reactivity allows selective protection in complex molecule assembly, enhancing stability during multi-step reactions. The chloromethyl functionality enables further derivatization through nucleophilic substitution, making it valuable in the design of pharmaceutical intermediates and functionalized silanes for materials science. It is also employed in the preparation of crosslinking agents for silicon-based polymers, contributing to improved thermal and mechanical properties in cured resins.

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