1-[Tris(1-methylethyl)silyl]-1H-pyrrolo[2,3-b]pyridine

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Reagent Code: #242998
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CAS Number 1093759-49-9

science Other reagents with same CAS 1093759-49-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 274.48 g/mol
Formula C₁₆H₂₆N₂Si
badge Registry Numbers
MDL Number MFCD09743456
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a specialized protecting group reagent in organic synthesis, particularly in the modification and stabilization of sensitive functional groups during multi-step reactions. Its bulky silyl structure provides steric shielding, which helps prevent unwanted side reactions in heterocyclic compounds. Commonly applied in pharmaceutical synthesis where selective protection of nitrogen-containing heterocycles is required. Exhibits good stability under various reaction conditions, making it valuable in the preparation of complex molecules such as kinase inhibitors and other bioactive agents.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,910.00
inventory 1g
10-20 days ฿7,960.00
inventory 100mg
10-20 days ฿1,730.00

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1-[Tris(1-methylethyl)silyl]-1H-pyrrolo[2,3-b]pyridine
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Used as a specialized protecting group reagent in organic synthesis, particularly in the modification and stabilization of sensitive functional groups during multi-step reactions. Its bulky silyl structure provides steric shielding, which helps prevent unwanted side reactions in heterocyclic compounds. Commonly applied in pharmaceutical synthesis where selective protection of nitrogen-containing heterocycles is required. Exhibits good stability under various reaction conditions, making it valuable in the

Used as a specialized protecting group reagent in organic synthesis, particularly in the modification and stabilization of sensitive functional groups during multi-step reactions. Its bulky silyl structure provides steric shielding, which helps prevent unwanted side reactions in heterocyclic compounds. Commonly applied in pharmaceutical synthesis where selective protection of nitrogen-containing heterocycles is required. Exhibits good stability under various reaction conditions, making it valuable in the preparation of complex molecules such as kinase inhibitors and other bioactive agents.

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