tert-butyl (4-((trimethylsilyl)ethynyl)benzyl)carbamate

98%

Reagent Code: #244900
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CAS Number 680190-95-8

science Other reagents with same CAS 680190-95-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 303.48 g/mol
Formula C₁₇H₂₅NO₂Si
thermostat Physical Properties
Melting Point 95-96 °C
inventory_2 Storage & Handling
Storage 2-8 °C, sealed, dry

description Product Description

Used in organic synthesis as a protected amine building block, particularly in pharmaceutical and agrochemical research. The tert-butyl carbamate (Boc) group provides stability and selective deprotection under mild acidic conditions, enabling stepwise construction of complex molecules. The trimethylsilyl-protected ethynyl moiety allows for further functionalization via click chemistry or palladium-catalyzed coupling reactions, making this compound valuable in the development of conjugated systems, fluorescent probes, and bioactive molecule synthesis. Its dual functionality supports modular design in drug discovery and materials science.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,240.00
inventory 250mg
10-20 days ฿4,470.00

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tert-butyl (4-((trimethylsilyl)ethynyl)benzyl)carbamate
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Used in organic synthesis as a protected amine building block, particularly in pharmaceutical and agrochemical research. The tert-butyl carbamate (Boc) group provides stability and selective deprotection under mild acidic conditions, enabling stepwise construction of complex molecules. The trimethylsilyl-protected ethynyl moiety allows for further functionalization via click chemistry or palladium-catalyzed coupling reactions, making this compound valuable in the development of conjugated systems, fluore

Used in organic synthesis as a protected amine building block, particularly in pharmaceutical and agrochemical research. The tert-butyl carbamate (Boc) group provides stability and selective deprotection under mild acidic conditions, enabling stepwise construction of complex molecules. The trimethylsilyl-protected ethynyl moiety allows for further functionalization via click chemistry or palladium-catalyzed coupling reactions, making this compound valuable in the development of conjugated systems, fluorescent probes, and bioactive molecule synthesis. Its dual functionality supports modular design in drug discovery and materials science.

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