(2S,4R)-Dibenzyl 4-hydroxypyrrolidine-1,2-dicarboxylate

95%

Reagent Code: #36563
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CAS Number 13500-53-3

science Other reagents with same CAS 13500-53-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 355.38 g/mol
Formula C₂₀H₂₁NO₅
badge Registry Numbers
MDL Number MFCD12407103
thermostat Physical Properties
Boiling Point 517.884°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This compound is primarily utilized in the field of organic synthesis as a chiral building block. Its stereochemistry makes it valuable for constructing complex molecules with specific spatial arrangements, particularly in the development of pharmaceuticals. It is often employed in the synthesis of biologically active compounds, including potential drug candidates, where precise chiral control is essential for efficacy and safety. Additionally, it serves as an intermediate in the preparation of peptidomimetics and other bioactive molecules, aiding in the study of enzyme interactions and receptor binding. Its versatility in asymmetric synthesis makes it a useful tool for researchers in medicinal chemistry and drug discovery.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿20,691.00
inventory 250mg
10-20 days ฿2,583.00
inventory 1g
10-20 days ฿6,462.00
inventory 100mg
10-20 days ฿1,728.00

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(2S,4R)-Dibenzyl 4-hydroxypyrrolidine-1,2-dicarboxylate
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This compound is primarily utilized in the field of organic synthesis as a chiral building block. Its stereochemistry makes it valuable for constructing complex molecules with specific spatial arrangements, particularly in the development of pharmaceuticals. It is often employed in the synthesis of biologically active compounds, including potential drug candidates, where precise chiral control is essential for efficacy and safety. Additionally, it serves as an intermediate in the preparation of peptidomi

This compound is primarily utilized in the field of organic synthesis as a chiral building block. Its stereochemistry makes it valuable for constructing complex molecules with specific spatial arrangements, particularly in the development of pharmaceuticals. It is often employed in the synthesis of biologically active compounds, including potential drug candidates, where precise chiral control is essential for efficacy and safety. Additionally, it serves as an intermediate in the preparation of peptidomimetics and other bioactive molecules, aiding in the study of enzyme interactions and receptor binding. Its versatility in asymmetric synthesis makes it a useful tool for researchers in medicinal chemistry and drug discovery.

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