Ethyl 1-phenylpiperidine-4-carboxylate
95%
Reagent
Code: #83135
CAS Number
247022-37-3
blur_circular Chemical Specifications
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Molecular Information
Weight
233.31 g/mol
Formula
C₁₄H₁₉NO₂
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Registry Numbers
MDL Number
MFCD21609276
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Physical Properties
Boiling Point
337.1±35.0 °C(Predicted)
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Storage & Handling
Density
1.081±0.06 g/cm3(Predicted)
Storage
Room temperature, sealed, dry
description Product Description
Ethyl 1-phenylpiperidine-4-carboxylate finds its primary application in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmaceutical compounds. It is particularly valuable in the development of central nervous system (CNS) drugs, where its structure serves as a building block for creating molecules with potential therapeutic effects. Researchers utilize it to design and synthesize analogs that may exhibit analgesic, anti-inflammatory, or neuroprotective properties. Additionally, its role in the production of compounds targeting neurotransmitter systems, such as dopamine or serotonin receptors, highlights its significance in drug discovery. Beyond pharmaceuticals, it is also explored in academic research for studying chemical reactions and developing novel synthetic pathways.
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Ethyl 1-phenylpiperidine-4-carboxylate
Ethyl 1-phenylpiperidine-4-carboxylate finds its primary application in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmaceutical compounds. It is particularly valuable in the development of central nervous system (CNS) drugs, where its structure serves as a building block for creating molecules with potential therapeutic effects. Researchers utilize it to design and synthesize analogs that may exhibit analgesic, anti-inflammatory, or neuroprotective properties. Additionally, its role in the production of compounds targeting neurotransmitter systems, such as dopamine or serotonin receptors, highlights its significance in drug discovery. Beyond pharmaceuticals, it is also explored in academic research for studying chemical reactions and developing novel synthetic pathways.
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