tert-butyl(3,5-difluorophenoxy)dimethylsilane

95%

Reagent Code: #240952
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CAS Number 917827-99-7

science Other reagents with same CAS 917827-99-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 244.34 g/mol
Formula C₁₂H₁₈F₂OSi
badge Registry Numbers
MDL Number MFCD23164074
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a silyl protecting group in organic synthesis, particularly in the pharmaceutical industry for the selective protection of phenolic hydroxyl groups. Its steric bulk and electron-withdrawing fluorine atoms enhance stability under various reaction conditions, making it valuable in multi-step syntheses where controlled deprotection is required. Commonly employed in the preparation of complex molecules such as drug intermediates and bioactive compounds, especially in routes involving sensitive functional groups.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿9,560.00
1g
10-20 days ฿26,870.00
tert-butyl(3,5-difluorophenoxy)dimethylsilane
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Used as a silyl protecting group in organic synthesis, particularly in the pharmaceutical industry for the selective protection of phenolic hydroxyl groups. Its steric bulk and electron-withdrawing fluorine atoms enhance stability under various reaction conditions, making it valuable in multi-step syntheses where controlled deprotection is required. Commonly employed in the preparation of complex molecules such as drug intermediates and bioactive compounds, especially in routes involving sensitive functi

Used as a silyl protecting group in organic synthesis, particularly in the pharmaceutical industry for the selective protection of phenolic hydroxyl groups. Its steric bulk and electron-withdrawing fluorine atoms enhance stability under various reaction conditions, making it valuable in multi-step syntheses where controlled deprotection is required. Commonly employed in the preparation of complex molecules such as drug intermediates and bioactive compounds, especially in routes involving sensitive functional groups.

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