Tert-butyl 3-(iodomethyl)pyrrolidine-1-carboxylate

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Reagent Code: #65087
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CAS Number 479622-36-1

science Other reagents with same CAS 479622-36-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 311.16 g/mol
Formula C₁₀H₁₈INO₂
badge Registry Numbers
MDL Number MFCD08059333
thermostat Physical Properties
Boiling Point 319°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, away from light, dry, sealed

description Product Description

This compound is primarily used in organic synthesis as a versatile intermediate for the construction of complex molecules. Its structure, featuring both a tert-butyl ester group and an iodo-methyl substituent, makes it valuable in the development of pharmaceuticals and bioactive compounds. The iodomethyl group serves as a reactive site for further functionalization, enabling coupling reactions or nucleophilic substitutions. Meanwhile, the tert-butyl ester acts as a protecting group for amines, which can be selectively removed under mild acidic conditions. This chemical is particularly useful in the synthesis of pyrrolidine-based compounds, which are common motifs in drug discovery, such as inhibitors, receptor antagonists, and enzyme modulators. Its application extends to the preparation of peptidomimetics and other biologically active molecules.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿864.00
inventory 250mg
10-20 days ฿1,548.00
inventory 1g
10-20 days ฿4,185.00

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Tert-butyl 3-(iodomethyl)pyrrolidine-1-carboxylate
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This compound is primarily used in organic synthesis as a versatile intermediate for the construction of complex molecules. Its structure, featuring both a tert-butyl ester group and an iodo-methyl substituent, makes it valuable in the development of pharmaceuticals and bioactive compounds. The iodomethyl group serves as a reactive site for further functionalization, enabling coupling reactions or nucleophilic substitutions. Meanwhile, the tert-butyl ester acts as a protecting group for amines, which can be
This compound is primarily used in organic synthesis as a versatile intermediate for the construction of complex molecules. Its structure, featuring both a tert-butyl ester group and an iodo-methyl substituent, makes it valuable in the development of pharmaceuticals and bioactive compounds. The iodomethyl group serves as a reactive site for further functionalization, enabling coupling reactions or nucleophilic substitutions. Meanwhile, the tert-butyl ester acts as a protecting group for amines, which can be selectively removed under mild acidic conditions. This chemical is particularly useful in the synthesis of pyrrolidine-based compounds, which are common motifs in drug discovery, such as inhibitors, receptor antagonists, and enzyme modulators. Its application extends to the preparation of peptidomimetics and other biologically active molecules.
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