1-(tert-butyl)-2-(methoxymethoxy)benzene

Reagent Code: #238908
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CAS Number 261903-04-2

science Other reagents with same CAS 261903-04-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 194.27 g/mol
Formula C₁₂H₁₈O₂
inventory_2 Storage & Handling
Storage -20 °C, Sealed, Drying, Inert Gas

description Product Description

Used as an intermediate in organic synthesis, particularly in pharmaceutical and agrochemical industries. Its protected phenol functionality makes it valuable in multi-step synthesis where selective reactions are required. The methoxymethoxy group acts as a protecting group for phenols, allowing other functional groups to be modified without interference. After desired transformations, the protecting group can be removed under mild acidic conditions to regenerate the phenol. This compound is also employed in the preparation of fragrances and functional materials due to its stability and reactivity profile.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,740.00
inventory 1g
10-20 days ฿7,700.00
1-(tert-butyl)-2-(methoxymethoxy)benzene
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Used as an intermediate in organic synthesis, particularly in pharmaceutical and agrochemical industries. Its protected phenol functionality makes it valuable in multi-step synthesis where selective reactions are required. The methoxymethoxy group acts as a protecting group for phenols, allowing other functional groups to be modified without interference. After desired transformations, the protecting group can be removed under mild acidic conditions to regenerate the phenol. This compound is also employe

Used as an intermediate in organic synthesis, particularly in pharmaceutical and agrochemical industries. Its protected phenol functionality makes it valuable in multi-step synthesis where selective reactions are required. The methoxymethoxy group acts as a protecting group for phenols, allowing other functional groups to be modified without interference. After desired transformations, the protecting group can be removed under mild acidic conditions to regenerate the phenol. This compound is also employed in the preparation of fragrances and functional materials due to its stability and reactivity profile.

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