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

≥95%

Reagent Code: #113567
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CAS Number 1234576-86-3

science Other reagents with same CAS 1234576-86-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 297.13 g/mol
Formula C₉H₁₆INO₂
badge Registry Numbers
MDL Number MFCD17015908
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, particularly in the development of pharmaceuticals and bioactive molecules. Its structure, featuring a pyrrolidine ring with an iodine substituent, makes it a valuable intermediate in the construction of complex organic compounds. The iodine atom serves as a reactive site for further functionalization through cross-coupling reactions, such as Suzuki or Sonogashira couplings, enabling the introduction of diverse chemical groups. Additionally, the tert-butyloxycarbonyl (Boc) protecting group enhances stability during synthetic processes and can be selectively removed under mild conditions, allowing for further modifications. This compound is often employed in the synthesis of chiral molecules, contributing to the production of enantiomerically pure drugs and other biologically active compounds. Its versatility and reactivity make it a key building block in medicinal chemistry and drug discovery research.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿6,615.00

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(R)-tert-Butyl 3-iodopyrrolidine-1-carboxylate
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This compound is primarily utilized in organic synthesis, particularly in the development of pharmaceuticals and bioactive molecules. Its structure, featuring a pyrrolidine ring with an iodine substituent, makes it a valuable intermediate in the construction of complex organic compounds. The iodine atom serves as a reactive site for further functionalization through cross-coupling reactions, such as Suzuki or Sonogashira couplings, enabling the introduction of diverse chemical groups. Additionally, the t

This compound is primarily utilized in organic synthesis, particularly in the development of pharmaceuticals and bioactive molecules. Its structure, featuring a pyrrolidine ring with an iodine substituent, makes it a valuable intermediate in the construction of complex organic compounds. The iodine atom serves as a reactive site for further functionalization through cross-coupling reactions, such as Suzuki or Sonogashira couplings, enabling the introduction of diverse chemical groups. Additionally, the tert-butyloxycarbonyl (Boc) protecting group enhances stability during synthetic processes and can be selectively removed under mild conditions, allowing for further modifications. This compound is often employed in the synthesis of chiral molecules, contributing to the production of enantiomerically pure drugs and other biologically active compounds. Its versatility and reactivity make it a key building block in medicinal chemistry and drug discovery research.

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