(11-Bromoundecyl)trichlorosilane

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Reagent Code: #147517
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CAS Number 79769-48-5

science Other reagents with same CAS 79769-48-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 368.64 g/mol
Formula C₁₁H₂₂BrCl₃Si
badge Registry Numbers
MDL Number MFCD00270977
thermostat Physical Properties
Boiling Point 65°C/40mmHg(lit.)
inventory_2 Storage & Handling
Density 1.26g/ml
Storage Room temperature, stored in inert gas

description Product Description

Used as a coupling agent in surface modification, particularly for introducing bromine-terminated alkyl chains onto silica or glass surfaces. The trichlorosilane group reacts readily with hydroxyl groups on these surfaces, forming stable siloxane bonds. The bromine end-group allows for further functionalization via nucleophilic substitution or metal-catalyzed coupling reactions, making it valuable in creating tailored interfaces for biosensors, nanotechnology, and organic-inorganic hybrid materials. Commonly employed in the preparation of self-assembled monolayers (SAMs) where controlled surface chemistry is required.

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Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿1,800.00
inventory 1g
10-20 days ฿6,300.00
inventory 5g
10-20 days ฿24,290.00

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(11-Bromoundecyl)trichlorosilane
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Used as a coupling agent in surface modification, particularly for introducing bromine-terminated alkyl chains onto silica or glass surfaces. The trichlorosilane group reacts readily with hydroxyl groups on these surfaces, forming stable siloxane bonds. The bromine end-group allows for further functionalization via nucleophilic substitution or metal-catalyzed coupling reactions, making it valuable in creating tailored interfaces for biosensors, nanotechnology, and organic-inorganic hybrid materials. Comm

Used as a coupling agent in surface modification, particularly for introducing bromine-terminated alkyl chains onto silica or glass surfaces. The trichlorosilane group reacts readily with hydroxyl groups on these surfaces, forming stable siloxane bonds. The bromine end-group allows for further functionalization via nucleophilic substitution or metal-catalyzed coupling reactions, making it valuable in creating tailored interfaces for biosensors, nanotechnology, and organic-inorganic hybrid materials. Commonly employed in the preparation of self-assembled monolayers (SAMs) where controlled surface chemistry is required.

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