(S)-tert-Butyl 3-iodopyrrolidine-1-carboxylate
97%
Reagent
Code: #113813
CAS Number
1234576-81-8
blur_circular Chemical Specifications
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Molecular Information
Weight
297.13 g/mol
Formula
C₉H₁₆INO₂
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Registry Numbers
MDL Number
MFCD17015907
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Physical Properties
Boiling Point
300.7±35.0°C at 760 mmHg
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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.
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(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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