Methyl 4-aminopiperidine-1-carboxylate

≥95%

Reagent Code: #209051
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CAS Number 1019351-46-2

science Other reagents with same CAS 1019351-46-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 158.20 g/mol
Formula C₇H₁₄N₂O₂
badge Registry Numbers
MDL Number MFCD11128922
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed from light

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) for central nervous system (CNS) disorders and psychiatric conditions. Its structure supports the creation of bioactive molecules due to the presence of both amine and ester functional groups, enabling diverse chemical modifications. Commonly employed in medicinal chemistry for constructing piperidine-based drug candidates, it contributes to improving metabolic stability and receptor binding affinity. Also utilized in the preparation of kinase inhibitors and other targeted therapies in oncology research. Its protected amine group allows for selective reactions, making it valuable in multi-step organic synthesis.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿780.00
inventory 250mg
10-20 days ฿1,920.00
inventory 1g
10-20 days ฿7,620.00

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Methyl 4-aminopiperidine-1-carboxylate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) for central nervous system (CNS) disorders and psychiatric conditions. Its structure supports the creation of bioactive molecules due to the presence of both amine and ester functional groups, enabling diverse chemical modifications. Commonly employed in medicinal chemistry for constructing piperidine-based drug candidates, it contributes to improving metabolic stabi

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) for central nervous system (CNS) disorders and psychiatric conditions. Its structure supports the creation of bioactive molecules due to the presence of both amine and ester functional groups, enabling diverse chemical modifications. Commonly employed in medicinal chemistry for constructing piperidine-based drug candidates, it contributes to improving metabolic stability and receptor binding affinity. Also utilized in the preparation of kinase inhibitors and other targeted therapies in oncology research. Its protected amine group allows for selective reactions, making it valuable in multi-step organic synthesis.

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