(3R,4S)-rel-tert-Butyl 3-hydroxy-4-methylpyrrolidine-1-carboxylate

97%

Reagent Code: #113239
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CAS Number 885102-33-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 201.26 g/mol
Formula C₁₀H₁₉NO₃
badge Registry Numbers
MDL Number MFCD18375158
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This compound is primarily utilized in the pharmaceutical industry as an intermediate in the synthesis of more complex molecules. It plays a crucial role in the development of various therapeutic agents, particularly in the creation of chiral drugs where specific stereochemistry is essential for biological activity. Its structure, featuring both hydroxyl and carboxylate functional groups, makes it a versatile building block for constructing pyrrolidine-based frameworks, which are common in many bioactive compounds. Additionally, it is employed in research settings for studying enzyme interactions and designing inhibitors that target specific biochemical pathways. Its stability and reactivity also make it suitable for use in organic synthesis, aiding in the production of fine chemicals and active pharmaceutical ingredients (APIs).

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Size Availability Unit Price Quantity
inventory 1g
10-20 days $611.06
inventory 100mg
10-20 days $152.23
inventory 250mg
10-20 days $243.56
(3R,4S)-rel-tert-Butyl 3-hydroxy-4-methylpyrrolidine-1-carboxylate
This compound is primarily utilized in the pharmaceutical industry as an intermediate in the synthesis of more complex molecules. It plays a crucial role in the development of various therapeutic agents, particularly in the creation of chiral drugs where specific stereochemistry is essential for biological activity. Its structure, featuring both hydroxyl and carboxylate functional groups, makes it a versatile building block for constructing pyrrolidine-based frameworks, which are common in many bioactive compounds. Additionally, it is employed in research settings for studying enzyme interactions and designing inhibitors that target specific biochemical pathways. Its stability and reactivity also make it suitable for use in organic synthesis, aiding in the production of fine chemicals and active pharmaceutical ingredients (APIs).
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