(S)-1-N-BOC-PIPERIDINE-2-ETHANOL

95%

Reagent Code: #235751
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CAS Number 199942-74-0

science Other reagents with same CAS 199942-74-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 229.3159 g/mol
Formula C₁₂H₂₃NO₃
badge Registry Numbers
MDL Number MFCD02683200
thermostat Physical Properties
Boiling Point 324.1 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.043 g/cm3
Storage 2-8°C, dry, sealed

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring stereochemical control. Its protected alcohol and amine functionalities allow selective reactions, making it valuable in multi-step organic synthesis. Commonly employed in the production of central nervous system agents, including antidepressants and antipsychotics, due to the piperidine scaffold’s prevalence in neuroactive compounds. The BOC-protected amine ensures stability during reactions and can be deprotected under mild acidic conditions to release the free amine for further derivatization.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,080.00
inventory 1g
10-20 days ฿4,210.00
(S)-1-N-BOC-PIPERIDINE-2-ETHANOL
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring stereochemical control. Its protected alcohol and amine functionalities allow selective reactions, making it valuable in multi-step organic synthesis. Commonly employed in the production of central nervous system agents, including antidepressants and antipsychotics, due to the piperidine scaffold’s prevalence in neuroactive compounds. The BOC-protected

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring stereochemical control. Its protected alcohol and amine functionalities allow selective reactions, making it valuable in multi-step organic synthesis. Commonly employed in the production of central nervous system agents, including antidepressants and antipsychotics, due to the piperidine scaffold’s prevalence in neuroactive compounds. The BOC-protected amine ensures stability during reactions and can be deprotected under mild acidic conditions to release the free amine for further derivatization.

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