Bis(2-((Tert-Butyldimethylsilyl)Oxy)Ethyl)Amine

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Reagent Code: #154564
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CAS Number 169527-49-5

science Other reagents with same CAS 169527-49-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 333.66 g/mol
Formula C₁₆H₃₉NO₂Si₂
badge Registry Numbers
MDL Number MFCD00048820
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Bis(2-((tert-butyldimethylsilyl)oxy)ethyl)amine is a protected derivative of N,N-bis(2-hydroxyethyl)amine, featuring two tert-butyldimethylsilyl (TBS) protecting groups on the hydroxyl moieties. It functions as a key building block and intermediate in organic synthesis, particularly for the modification and assembly of nucleosides and oligonucleotides. The TBS groups offer steric protection and chemical stability, enabling selective functionalization at the amine site during the construction of complex biomolecules like RNA and DNA analogs. This compound is essential in solid-phase oligonucleotide synthesis and pharmaceutical applications, facilitating precise molecular architecture. It is widely used to prepare silyl-protected linkers and intermediates for coupling reactions in the production of antisense oligonucleotides, siRNA therapeutics, and related nucleic acid-based drugs.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿3,550.00
inventory 5g
10-20 days ฿10,560.00

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Bis(2-((Tert-Butyldimethylsilyl)Oxy)Ethyl)Amine
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Bis(2-((tert-butyldimethylsilyl)oxy)ethyl)amine is a protected derivative of N,N-bis(2-hydroxyethyl)amine, featuring two tert-butyldimethylsilyl (TBS) protecting groups on the hydroxyl moieties. It functions as a key building block and intermediate in organic synthesis, particularly for the modification and assembly of nucleosides and oligonucleotides. The TBS groups offer steric protection and chemical stability, enabling selective functionalization at the amine site during the construction of complex b

Bis(2-((tert-butyldimethylsilyl)oxy)ethyl)amine is a protected derivative of N,N-bis(2-hydroxyethyl)amine, featuring two tert-butyldimethylsilyl (TBS) protecting groups on the hydroxyl moieties. It functions as a key building block and intermediate in organic synthesis, particularly for the modification and assembly of nucleosides and oligonucleotides. The TBS groups offer steric protection and chemical stability, enabling selective functionalization at the amine site during the construction of complex biomolecules like RNA and DNA analogs. This compound is essential in solid-phase oligonucleotide synthesis and pharmaceutical applications, facilitating precise molecular architecture. It is widely used to prepare silyl-protected linkers and intermediates for coupling reactions in the production of antisense oligonucleotides, siRNA therapeutics, and related nucleic acid-based drugs.

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