tert-butyl(2-iodoethoxy)diphenylsilane

98%

Reagent Code: #244574
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CAS Number 126822-71-7

science Other reagents with same CAS 126822-71-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 410.36 g/mol
Formula C₁₈H₂₃IOSi
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical industries. Its primary application lies in its role as a silyl protecting group reagent, where it effectively masks hydroxyl groups during multi-step syntheses. The tert-butyl(2-iodoethoxy)diphenylsilane group offers high stability under various reaction conditions and can be selectively removed when needed, making it valuable in the construction of sensitive or sterically hindered compounds. The presence of the iodine atom allows for further functionalization via cross-coupling reactions, enabling the introduction of additional molecular fragments. This feature is especially useful in the development of bioactive molecules where precise structural control is required.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,070.00
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tert-butyl(2-iodoethoxy)diphenylsilane
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Used as a key intermediate in the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical industries. Its primary application lies in its role as a silyl protecting group reagent, where it effectively masks hydroxyl groups during multi-step syntheses. The tert-butyl(2-iodoethoxy)diphenylsilane group offers high stability under various reaction conditions and can be selectively removed when needed, making it valuable in the construction of sensitive or sterically hindered c

Used as a key intermediate in the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical industries. Its primary application lies in its role as a silyl protecting group reagent, where it effectively masks hydroxyl groups during multi-step syntheses. The tert-butyl(2-iodoethoxy)diphenylsilane group offers high stability under various reaction conditions and can be selectively removed when needed, making it valuable in the construction of sensitive or sterically hindered compounds. The presence of the iodine atom allows for further functionalization via cross-coupling reactions, enabling the introduction of additional molecular fragments. This feature is especially useful in the development of bioactive molecules where precise structural control is required.

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