(S)-Benzyl 2-methyl-4-oxopiperidine-1-carboxylate

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Reagent Code: #232481
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CAS Number 921599-74-8

science Other reagents with same CAS 921599-74-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 247.29 g/mol
Formula C₁₄H₁₇NO₃
badge Registry Numbers
MDL Number MFCD16660834
thermostat Physical Properties
Boiling Point 388.1±42.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.164±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry, light-proof

description Product Description

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of centrally acting agents such as dopamine receptor modulators. Its piperidine backbone with a protected amine and ketone functionality allows for selective modifications, making it valuable in medicinal chemistry for constructing bioactive molecules. Commonly employed in asymmetric synthesis routes where the (S)-configuration is critical for biological activity. Also utilized in the preparation of protease inhibitors and neuroactive compounds due to its structural similarity to natural alkaloids.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿24,400.00

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(S)-Benzyl 2-methyl-4-oxopiperidine-1-carboxylate
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Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of centrally acting agents such as dopamine receptor modulators. Its piperidine backbone with a protected amine and ketone functionality allows for selective modifications, making it valuable in medicinal chemistry for constructing bioactive molecules. Commonly employed in asymmetric synthesis routes where the (S)-configuration is critical for biological activity. Also utilized in the preparation of proteas

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of centrally acting agents such as dopamine receptor modulators. Its piperidine backbone with a protected amine and ketone functionality allows for selective modifications, making it valuable in medicinal chemistry for constructing bioactive molecules. Commonly employed in asymmetric synthesis routes where the (S)-configuration is critical for biological activity. Also utilized in the preparation of protease inhibitors and neuroactive compounds due to its structural similarity to natural alkaloids.

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