(R)-tert-Butyl piperidin-3-ylcarbamate hydrochloride

97%

Reagent Code: #230509
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CAS Number 1217656-59-1

science Other reagents with same CAS 1217656-59-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 236.74 g/mol
Formula C₁₀H₂₁ClN₂O₂
badge Registry Numbers
MDL Number MFCD08275943
inventory_2 Storage & Handling
Storage Store in an inert gas at room temperature

description Product Description

Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) that require high enantiomeric purity. Its protected amine group allows for selective reactions in multi-step organic syntheses, making it valuable in the production of central nervous system agents, including certain antidepressants and antipsychotics. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its rigid piperidine scaffold and defined stereochemistry. Also utilized in the preparation of enzyme inhibitors and receptor modulators where stereochemistry influences biological activity.

Available Sizes & Pricing

Size Availability Unit Price Quantity
5g
10-20 days ฿630.00
10g
10-20 days ฿1,100.00
25g
10-20 days ฿1,370.00
(R)-tert-Butyl piperidin-3-ylcarbamate hydrochloride
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Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) that require high enantiomeric purity. Its protected amine group allows for selective reactions in multi-step organic syntheses, making it valuable in the production of central nervous system agents, including certain antidepressants and antipsychotics. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its rigid

Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) that require high enantiomeric purity. Its protected amine group allows for selective reactions in multi-step organic syntheses, making it valuable in the production of central nervous system agents, including certain antidepressants and antipsychotics. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its rigid piperidine scaffold and defined stereochemistry. Also utilized in the preparation of enzyme inhibitors and receptor modulators where stereochemistry influences biological activity.

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