trans-1-tert-Butyl 3-ethyl 4-aminopyrrolidine-1,3-dicarboxylate

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Reagent Code: #53189
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CAS Number 362489-56-3

science Other reagents with same CAS 362489-56-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 258.31 g/mol
Formula C₁₂H₂₂N₂O₄
badge Registry Numbers
MDL Number MFCD03839870
thermostat Physical Properties
Boiling Point 336.5°C at 760 mmHg
inventory_2 Storage & Handling
Density 1.129g/cm3
Storage 2-8°C, dry and sealed away from light

description Product Description

This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of biologically active molecules. Its structure, featuring both amino and carboxylate groups, makes it a versatile building block in organic synthesis. It is often employed in the preparation of pyrrolidine derivatives, which are key components in drugs targeting neurological disorders, such as Alzheimer's disease and Parkinson's disease. Additionally, it serves as a precursor in the creation of ligands for asymmetric catalysis, enhancing the efficiency of chiral synthesis in drug manufacturing. Its stability and reactivity also make it suitable for use in combinatorial chemistry for high-throughput screening of potential drug candidates.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿3,258.00
inventory 100mg
10-20 days ฿5,265.00
inventory 250mg
10-20 days ฿8,388.00

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trans-1-tert-Butyl 3-ethyl 4-aminopyrrolidine-1,3-dicarboxylate
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This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of biologically active molecules. Its structure, featuring both amino and carboxylate groups, makes it a versatile building block in organic synthesis. It is often employed in the preparation of pyrrolidine derivatives, which are key components in drugs targeting neurological disorders, such as Alzheimer's disease and Parkinson's disease. Additionally, it serves as a precursor in the creatio
This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of biologically active molecules. Its structure, featuring both amino and carboxylate groups, makes it a versatile building block in organic synthesis. It is often employed in the preparation of pyrrolidine derivatives, which are key components in drugs targeting neurological disorders, such as Alzheimer's disease and Parkinson's disease. Additionally, it serves as a precursor in the creation of ligands for asymmetric catalysis, enhancing the efficiency of chiral synthesis in drug manufacturing. Its stability and reactivity also make it suitable for use in combinatorial chemistry for high-throughput screening of potential drug candidates.
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