[3-[[tert-Butyl(dimethyl)silyl]oxymethyl]-1,2,3,5,6,7-hexahydropyrrolizin-8-yl]methanol

97%

Reagent Code: #130619
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CAS Number 1788873-94-8

science Other reagents with same CAS 1788873-94-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 285.5 g/mol
Formula C₁₅H₃₁NO₂Si
badge Registry Numbers
MDL Number MFCD31926127
thermostat Physical Properties
Boiling Point 328.3±7.0 °C(Predicted)
inventory_2 Storage & Handling
Density 0.99±0.1 g/cm3(Predicted)
Storage Room temperature, light-proof, inert gas

description Product Description

Used in organic synthesis as a protected intermediate in the preparation of complex natural products and bioactive molecules. The silyl ether group provides stability and selectivity during multi-step reactions, particularly in alkaloid synthesis. Its hydroxyl groups can be selectively deprotected and functionalized, making it valuable in pharmaceutical research for building intricate molecular architectures. Commonly employed in the development of enzyme inhibitors and neuroactive compounds due to its rigid, polycyclic framework.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿13,060.00
inventory 250mg
10-20 days ฿20,850.00
[3-[[tert-Butyl(dimethyl)silyl]oxymethyl]-1,2,3,5,6,7-hexahydropyrrolizin-8-yl]methanol
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Used in organic synthesis as a protected intermediate in the preparation of complex natural products and bioactive molecules. The silyl ether group provides stability and selectivity during multi-step reactions, particularly in alkaloid synthesis. Its hydroxyl groups can be selectively deprotected and functionalized, making it valuable in pharmaceutical research for building intricate molecular architectures. Commonly employed in the development of enzyme inhibitors and neuroactive compounds due to its r

Used in organic synthesis as a protected intermediate in the preparation of complex natural products and bioactive molecules. The silyl ether group provides stability and selectivity during multi-step reactions, particularly in alkaloid synthesis. Its hydroxyl groups can be selectively deprotected and functionalized, making it valuable in pharmaceutical research for building intricate molecular architectures. Commonly employed in the development of enzyme inhibitors and neuroactive compounds due to its rigid, polycyclic framework.

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