2-(tert-Butyldimethylsilyl)isoindoline-1,3-dione

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Reagent Code: #132085
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CAS Number 79293-84-8

science Other reagents with same CAS 79293-84-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 261.39 g/mol
Formula C₁₄H₁₉NO₂Si
badge Registry Numbers
MDL Number MFCD00674006
thermostat Physical Properties
Melting Point 115-119 °C(lit.)
Boiling Point 336.0±25.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.09±0.1 g/cm3(Predicted)
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used as a protected amine building block in organic synthesis, particularly in pharmaceutical and agrochemical industries. The tert-butyldimethylsilyl (TBS) group acts as a protecting group for the amine functionality, allowing selective reactions at other sites in the molecule. This compound is especially useful in multi-step syntheses where controlled deprotection is needed under mild conditions. Its stability under various reaction conditions makes it valuable in peptide synthesis and in the preparation of nitrogen-containing heterocycles. Commonly employed in research settings for the development of active pharmaceutical ingredients (APIs).

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,030.00
inventory 1g
10-20 days ฿8,160.00
inventory 5g
10-20 days ฿29,080.00

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2-(tert-Butyldimethylsilyl)isoindoline-1,3-dione
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Used as a protected amine building block in organic synthesis, particularly in pharmaceutical and agrochemical industries. The tert-butyldimethylsilyl (TBS) group acts as a protecting group for the amine functionality, allowing selective reactions at other sites in the molecule. This compound is especially useful in multi-step syntheses where controlled deprotection is needed under mild conditions. Its stability under various reaction conditions makes it valuable in peptide synthesis and in the preparati

Used as a protected amine building block in organic synthesis, particularly in pharmaceutical and agrochemical industries. The tert-butyldimethylsilyl (TBS) group acts as a protecting group for the amine functionality, allowing selective reactions at other sites in the molecule. This compound is especially useful in multi-step syntheses where controlled deprotection is needed under mild conditions. Its stability under various reaction conditions makes it valuable in peptide synthesis and in the preparation of nitrogen-containing heterocycles. Commonly employed in research settings for the development of active pharmaceutical ingredients (APIs).

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