(2S,5R)-Benzyl 5-amino-2-methylpiperidine-1-carboxylate hydrochloride

97%

Reagent Code: #237509
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CAS Number 1207853-23-3

science Other reagents with same CAS 1207853-23-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 284.78 g/mol
Formula C₁₄H₂₁ClN₂O₂
badge Registry Numbers
MDL Number MFCD22689536
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of protease inhibitors and central nervous system (CNS) active compounds. Its stereochemistry enables selective interactions in drug design, improving potency and reducing off-target effects. Commonly employed in the preparation of antiviral medications, including certain hepatitis C and HIV treatments. Also utilized in the construction of complex piperidine-based scaffolds for medicinal chemistry research, aiding in the optimization of pharmacokinetic properties such as metabolic stability and bioavailability.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,400.00
inventory 250mg
10-20 days ฿2,390.00
inventory 1g
10-20 days ฿7,180.00
inventory 5g
10-20 days ฿31,050.00

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(2S,5R)-Benzyl 5-amino-2-methylpiperidine-1-carboxylate hydrochloride
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Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of protease inhibitors and central nervous system (CNS) active compounds. Its stereochemistry enables selective interactions in drug design, improving potency and reducing off-target effects. Commonly employed in the preparation of antiviral medications, including certain hepatitis C and HIV treatments. Also utilized in the construction of complex piperidine-based scaffolds for medicinal chemistry

Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of protease inhibitors and central nervous system (CNS) active compounds. Its stereochemistry enables selective interactions in drug design, improving potency and reducing off-target effects. Commonly employed in the preparation of antiviral medications, including certain hepatitis C and HIV treatments. Also utilized in the construction of complex piperidine-based scaffolds for medicinal chemistry research, aiding in the optimization of pharmacokinetic properties such as metabolic stability and bioavailability.

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