1-Methoxy-3-trimethylsilyloxybenzene

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Reagent Code: #203912
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CAS Number 33285-71-1

science Other reagents with same CAS 33285-71-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 196.32 g/mol
Formula C₁₀H₁₆O₂Si
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in organic synthesis, particularly in the preparation of substituted aromatic compounds. It serves as a protected form of a resorcinol derivative, enabling selective reactions on aromatic rings without interference from reactive hydroxyl groups. Commonly employed in pharmaceutical synthesis and fine chemical manufacturing where controlled functionalization of benzene rings is required. The trimethylsilyl and methoxy groups act as orthogonal protecting groups, allowing stepwise deprotection and modification. Also utilized in the development of fragrances and functional materials due to its stability and reactivity profile.

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inventory 1g
10-20 days ฿20,000.00

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1-Methoxy-3-trimethylsilyloxybenzene
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Used as a key intermediate in organic synthesis, particularly in the preparation of substituted aromatic compounds. It serves as a protected form of a resorcinol derivative, enabling selective reactions on aromatic rings without interference from reactive hydroxyl groups. Commonly employed in pharmaceutical synthesis and fine chemical manufacturing where controlled functionalization of benzene rings is required. The trimethylsilyl and methoxy groups act as orthogonal protecting groups, allowing stepwise

Used as a key intermediate in organic synthesis, particularly in the preparation of substituted aromatic compounds. It serves as a protected form of a resorcinol derivative, enabling selective reactions on aromatic rings without interference from reactive hydroxyl groups. Commonly employed in pharmaceutical synthesis and fine chemical manufacturing where controlled functionalization of benzene rings is required. The trimethylsilyl and methoxy groups act as orthogonal protecting groups, allowing stepwise deprotection and modification. Also utilized in the development of fragrances and functional materials due to its stability and reactivity profile.

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