1-tert-Butyl 4-ethyl 4-(aminomethyl)piperidine-1,4-dicarboxylate

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Reagent Code: #39585
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CAS Number 1016258-69-7

science Other reagents with same CAS 1016258-69-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 286.37 g/mol
Formula C₁₄H₂₆N₂O₄
badge Registry Numbers
MDL Number MFCD14525454
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in an inert gas

description Product Description

This compound is primarily utilized in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) targeting neurological and psychiatric disorders. Its structure, featuring both tert-butyl and ethyl ester groups, makes it a valuable intermediate in the creation of molecules that interact with neurotransmitter systems, such as those involving dopamine or serotonin receptors. Additionally, it is employed in the preparation of prodrugs, where its ester groups can be hydrolyzed to release the active drug in vivo. Its piperidine core is also significant in designing compounds with improved bioavailability and metabolic stability, making it a key building block in medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿18,909.00
inventory 1g
10-20 days ฿6,282.00
inventory 250mg
10-20 days ฿2,511.00

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1-tert-Butyl 4-ethyl 4-(aminomethyl)piperidine-1,4-dicarboxylate
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This compound is primarily utilized in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) targeting neurological and psychiatric disorders. Its structure, featuring both tert-butyl and ethyl ester groups, makes it a valuable intermediate in the creation of molecules that interact with neurotransmitter systems, such as those involving dopamine or serotonin receptors. Additionally, it is employed in the preparation of prodrugs, where its ester grou

This compound is primarily utilized in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) targeting neurological and psychiatric disorders. Its structure, featuring both tert-butyl and ethyl ester groups, makes it a valuable intermediate in the creation of molecules that interact with neurotransmitter systems, such as those involving dopamine or serotonin receptors. Additionally, it is employed in the preparation of prodrugs, where its ester groups can be hydrolyzed to release the active drug in vivo. Its piperidine core is also significant in designing compounds with improved bioavailability and metabolic stability, making it a key building block in medicinal chemistry.

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