(2R,4S)-rel-tert-Butyl 4-hydroxy-2-methylpiperidine-1-carboxylate

95%

Reagent Code: #232205
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CAS Number 152491-46-8

science Other reagents with same CAS 152491-46-8

blur_circular Chemical Specifications

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Weight 215.293 g/mol
Formula C₁₁H₂₁NO₃
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of centrally acting agents such as antipsychotics and antidepressants. Its stereochemistry allows for selective interaction with biological targets, enhancing drug efficacy and reducing side effects. Commonly employed in the preparation of active pharmaceutical ingredients (APIs) requiring a piperidine scaffold with defined stereochemistry. Also utilized in research settings for the design of enzyme inhibitors and receptor modulators due to its structural stability and functional versatility.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,930.00
inventory 1g
10-20 days ฿7,310.00
inventory 5g
10-20 days ฿29,560.00

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(2R,4S)-rel-tert-Butyl 4-hydroxy-2-methylpiperidine-1-carboxylate
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Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of centrally acting agents such as antipsychotics and antidepressants. Its stereochemistry allows for selective interaction with biological targets, enhancing drug efficacy and reducing side effects. Commonly employed in the preparation of active pharmaceutical ingredients (APIs) requiring a piperidine scaffold with defined stereochemistry. Also utilized in research settings for the design of enzyme inh

Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of centrally acting agents such as antipsychotics and antidepressants. Its stereochemistry allows for selective interaction with biological targets, enhancing drug efficacy and reducing side effects. Commonly employed in the preparation of active pharmaceutical ingredients (APIs) requiring a piperidine scaffold with defined stereochemistry. Also utilized in research settings for the design of enzyme inhibitors and receptor modulators due to its structural stability and functional versatility.

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