(3R,4S)-tert-butyl 3-allyl-4-hydroxypyrrolidine-1-carboxylate

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Reagent Code: #52252
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CAS Number 120871-72-9

science Other reagents with same CAS 120871-72-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 227.3 g/mol
Formula C₁₂H₂₁NO₃
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

This compound is primarily utilized in the synthesis of complex organic molecules, particularly in pharmaceutical research. It serves as a key intermediate in the development of biologically active compounds, such as inhibitors or modulators for specific enzymes or receptors. Its structure, featuring both a hydroxyl group and an allyl group, makes it versatile for further functionalization, enabling the creation of diverse chemical entities. Additionally, it is often employed in asymmetric synthesis due to its chiral centers, which are crucial for producing enantiomerically pure substances. This compound is also valuable in medicinal chemistry for constructing pyrrolidine-based scaffolds, which are common in drug discovery for their pharmacological properties.

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Size Availability Unit Price Quantity
inventory 0.1g
10-20 days ฿7,308.00
inventory 0.25g
10-20 days ฿12,186.00
inventory 1g
10-20 days ฿30,474.00

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(3R,4S)-tert-butyl 3-allyl-4-hydroxypyrrolidine-1-carboxylate
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This compound is primarily utilized in the synthesis of complex organic molecules, particularly in pharmaceutical research. It serves as a key intermediate in the development of biologically active compounds, such as inhibitors or modulators for specific enzymes or receptors. Its structure, featuring both a hydroxyl group and an allyl group, makes it versatile for further functionalization, enabling the creation of diverse chemical entities. Additionally, it is often employed in asymmetric synthesis due to its chiral centers, which are crucial for producing enantiomerically pure substances. This compound is also valuable in medicinal chemistry for constructing pyrrolidine-based scaffolds, which are common in drug discovery for their pharmacological properties.
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