Ethyl (2r,4r)-4-methyl-2-piperidinecarboxylate l-tartarate

95%

Reagent Code: #229547
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CAS Number 131278-84-7

science Other reagents with same CAS 131278-84-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 321.32 g/mol
Formula C₁₃H₂₃NO₈
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in pharmaceutical synthesis as a chiral building block for developing active pharmaceutical ingredients (APIs), particularly in the production of neurologically active compounds. Its stereochemistry makes it valuable in creating enantioselective drugs, where specific 3D orientation is critical for biological activity. Commonly employed in research and development of medications targeting central nervous system disorders. Also utilized in asymmetric synthesis to introduce chiral centers in complex molecules. The tartarate salt form enhances stability and crystallinity, facilitating purification and handling during manufacturing processes.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿4,100.00
inventory 10g
10-20 days ฿6,200.00
inventory 25g
10-20 days ฿12,340.00
inventory 50g
10-20 days ฿20,600.00
inventory 100g
10-20 days ฿30,900.00
inventory 500g
10-20 days ฿123,560.00

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Ethyl (2r,4r)-4-methyl-2-piperidinecarboxylate l-tartarate
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Used in pharmaceutical synthesis as a chiral building block for developing active pharmaceutical ingredients (APIs), particularly in the production of neurologically active compounds. Its stereochemistry makes it valuable in creating enantioselective drugs, where specific 3D orientation is critical for biological activity. Commonly employed in research and development of medications targeting central nervous system disorders. Also utilized in asymmetric synthesis to introduce chiral centers in complex mo

Used in pharmaceutical synthesis as a chiral building block for developing active pharmaceutical ingredients (APIs), particularly in the production of neurologically active compounds. Its stereochemistry makes it valuable in creating enantioselective drugs, where specific 3D orientation is critical for biological activity. Commonly employed in research and development of medications targeting central nervous system disorders. Also utilized in asymmetric synthesis to introduce chiral centers in complex molecules. The tartarate salt form enhances stability and crystallinity, facilitating purification and handling during manufacturing processes.

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