(R)-tert-Butyl 3-(iodomethyl)pyrrolidine-1-carboxylate

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Reagent Code: #82970
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CAS Number 1187932-69-9

science Other reagents with same CAS 1187932-69-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 311.16 g/mol
Formula C₁₀H₁₈INO₂
badge Registry Numbers
MDL Number MFCD08059332
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored under inert gas

description Product Description

This compound is primarily utilized in organic synthesis as a versatile intermediate for the construction of complex molecules, particularly in pharmaceutical research. Its structure, featuring both a pyrrolidine ring and an iodomethyl group, makes it valuable for introducing functionalized pyrrolidine moieties into target molecules. The iodine atom serves as a reactive site for further transformations, such as cross-coupling reactions, enabling the formation of carbon-carbon bonds. Additionally, the tert-butyloxycarbonyl (Boc) protecting group ensures stability during synthetic processes and can be easily removed when needed. This chemical is often employed in the development of bioactive compounds, including potential drug candidates, where the pyrrolidine scaffold is a key structural element.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,592.00
inventory 250mg
10-20 days ฿19,530.00

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(R)-tert-Butyl 3-(iodomethyl)pyrrolidine-1-carboxylate
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This compound is primarily utilized in organic synthesis as a versatile intermediate for the construction of complex molecules, particularly in pharmaceutical research. Its structure, featuring both a pyrrolidine ring and an iodomethyl group, makes it valuable for introducing functionalized pyrrolidine moieties into target molecules. The iodine atom serves as a reactive site for further transformations, such as cross-coupling reactions, enabling the formation of carbon-carbon bonds. Additionally, the tert-butyloxycarbonyl (Boc) protecting group ensures stability during synthetic processes and can be easily removed when needed. This chemical is often employed in the development of bioactive compounds, including potential drug candidates, where the pyrrolidine scaffold is a key structural element.
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