(S)-tert-Butyl 3-iodopyrrolidine-1-carboxylate

97%

Reagent Code: #113813
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CAS Number 1234576-81-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 297.13 g/mol
Formula C₉H₁₆INO₂
badge Registry Numbers
MDL Number MFCD17015907
thermostat Physical Properties
Boiling Point 300.7±35.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed away from light

description Product Description

This compound is primarily utilized in organic synthesis as a versatile intermediate. It is particularly valuable in the construction of complex molecules, especially in the pharmaceutical industry, where it serves as a building block for the development of active pharmaceutical ingredients (APIs). Its stereochemistry and functional groups make it suitable for use in asymmetric synthesis, enabling the creation of chiral compounds with high enantiomeric purity. Additionally, it is employed in the synthesis of pyrrolidine-based structures, which are common in various biologically active compounds. Its iodine moiety also allows for further functionalization through cross-coupling reactions, expanding its utility in medicinal chemistry and drug discovery.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿35,190.00
inventory 100mg
10-20 days ฿8,397.00
inventory 250mg
10-20 days ฿14,670.00
(S)-tert-Butyl 3-iodopyrrolidine-1-carboxylate
This compound is primarily utilized in organic synthesis as a versatile intermediate. It is particularly valuable in the construction of complex molecules, especially in the pharmaceutical industry, where it serves as a building block for the development of active pharmaceutical ingredients (APIs). Its stereochemistry and functional groups make it suitable for use in asymmetric synthesis, enabling the creation of chiral compounds with high enantiomeric purity. Additionally, it is employed in the synthesis of pyrrolidine-based structures, which are common in various biologically active compounds. Its iodine moiety also allows for further functionalization through cross-coupling reactions, expanding its utility in medicinal chemistry and drug discovery.
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