trans-Ethyl 1-benzyl-4-methylpyrrolidine-3-carboxylate

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Reagent Code: #54603
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CAS Number 261896-27-9

science Other reagents with same CAS 261896-27-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 247.33 g/mol
Formula C₁₅H₂₁NO₂
badge Registry Numbers
MDL Number MFCD13190627
thermostat Physical Properties
Boiling Point 302.2±35.0°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, where it serves as a key intermediate in the production of various pharmaceuticals. Its structure is particularly valuable in the development of compounds with potential therapeutic effects, such as those targeting neurological disorders. The presence of both benzyl and ester functional groups allows for further chemical modifications, making it versatile in drug discovery processes. Additionally, it has been explored in the synthesis of alkaloid-like molecules, which are of significant interest due to their biological activities. Researchers also leverage its chiral centers in asymmetric synthesis to create enantiomerically pure substances, which are crucial in the development of more effective and safer medications.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,142.00
inventory 100mg
10-20 days ฿1,440.00

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trans-Ethyl 1-benzyl-4-methylpyrrolidine-3-carboxylate
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This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmaceuticals. Its structure is particularly valuable in the development of compounds with potential therapeutic effects, such as those targeting neurological disorders. The presence of both benzyl and ester functional groups allows for further chemical modifications, making it versatile in drug discovery processes. Additionally, it has been explored in the synthesis

This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmaceuticals. Its structure is particularly valuable in the development of compounds with potential therapeutic effects, such as those targeting neurological disorders. The presence of both benzyl and ester functional groups allows for further chemical modifications, making it versatile in drug discovery processes. Additionally, it has been explored in the synthesis of alkaloid-like molecules, which are of significant interest due to their biological activities. Researchers also leverage its chiral centers in asymmetric synthesis to create enantiomerically pure substances, which are crucial in the development of more effective and safer medications.

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