Ethyl (2R,3S)-2-(4-(Cyclopentylamino)Phenyl)Piperidine-3-Carboxylate (2R,3R)-2,3-Bis((4-Methylbenzoyl)Oxy)Succinate

97%

Reagent Code: #185602
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CAS Number 1893415-79-6

science Other reagents with same CAS 1893415-79-6

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scatter_plot Molecular Information
Weight 544.57 g/mol
Formula C₂₀H₁₈O₈.₁/₂ C₁₉H₂₈N₂O₂
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used primarily in pharmaceutical research as a chiral intermediate in the synthesis of complex bioactive molecules. Its stereochemistry makes it valuable for developing enantioselective drugs, particularly in central nervous system agents and receptor-targeted therapies. The ester and amine functionalities allow for further chemical modifications, enabling the creation of prodrugs or improved pharmacokinetic profiles. It is also employed in structure-activity relationship (SAR) studies to optimize drug candidates.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,210.00
inventory 250mg
10-20 days ฿18,680.00
inventory 1g
10-20 days ฿29,380.00

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Ethyl (2R,3S)-2-(4-(Cyclopentylamino)Phenyl)Piperidine-3-Carboxylate (2R,3R)-2,3-Bis((4-Methylbenzoyl)Oxy)Succinate
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Used primarily in pharmaceutical research as a chiral intermediate in the synthesis of complex bioactive molecules. Its stereochemistry makes it valuable for developing enantioselective drugs, particularly in central nervous system agents and receptor-targeted therapies. The ester and amine functionalities allow for further chemical modifications, enabling the creation of prodrugs or improved pharmacokinetic profiles. It is also employed in structure-activity relationship (SAR) studies to optimize drug c

Used primarily in pharmaceutical research as a chiral intermediate in the synthesis of complex bioactive molecules. Its stereochemistry makes it valuable for developing enantioselective drugs, particularly in central nervous system agents and receptor-targeted therapies. The ester and amine functionalities allow for further chemical modifications, enabling the creation of prodrugs or improved pharmacokinetic profiles. It is also employed in structure-activity relationship (SAR) studies to optimize drug candidates.

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