6-(((tert-Butyldimethylsilyl)oxy)methyl)-2,2,3,3,9,9,10,10-octamethyl-4,8-dioxa-3,9-disilaundecan-6-amine

95%

Reagent Code: #124418
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CAS Number 35842-47-4

science Other reagents with same CAS 35842-47-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 463.92 g/mol
Formula C₂₂H₅₃NO₃Si₃
badge Registry Numbers
MDL Number MFCD22574795
inventory_2 Storage & Handling
Storage Room temperature, dark, inert gas

description Product Description

This compound is a specialized organic intermediate featuring a primary amine and a tert-butyldimethylsilyl (TBDMS)-protected hydroxymethyl group. It is employed in advanced organic synthesis, particularly for constructing complex molecules where selective reactivity at the amine is required while the alcohol functionality is masked to avoid side reactions. The TBDMS protection ensures stability under a range of conditions, including basic and aprotic environments, and can be selectively removed using fluoride sources. It is especially useful in peptide synthesis, nucleoside analogs, and pharmaceutical intermediate preparation, enabling efficient multi-step transformations with high yields and purity.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿5,400.00
inventory 250mg
10-20 days ฿1,998.00

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6-(((tert-Butyldimethylsilyl)oxy)methyl)-2,2,3,3,9,9,10,10-octamethyl-4,8-dioxa-3,9-disilaundecan-6-amine
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This compound is a specialized organic intermediate featuring a primary amine and a tert-butyldimethylsilyl (TBDMS)-protected hydroxymethyl group. It is employed in advanced organic synthesis, particularly for constructing complex molecules where selective reactivity at the amine is required while the alcohol functionality is masked to avoid side reactions. The TBDMS protection ensures stability under a range of conditions, including basic and aprotic environments, and can be selectively removed using fl

This compound is a specialized organic intermediate featuring a primary amine and a tert-butyldimethylsilyl (TBDMS)-protected hydroxymethyl group. It is employed in advanced organic synthesis, particularly for constructing complex molecules where selective reactivity at the amine is required while the alcohol functionality is masked to avoid side reactions. The TBDMS protection ensures stability under a range of conditions, including basic and aprotic environments, and can be selectively removed using fluoride sources. It is especially useful in peptide synthesis, nucleoside analogs, and pharmaceutical intermediate preparation, enabling efficient multi-step transformations with high yields and purity.

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