(R)-Benzyl 3-formylpiperidine-1-carboxylate

≥95%

Reagent Code: #230456
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CAS Number 435275-28-8

science Other reagents with same CAS 435275-28-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 247.29 g/mol
Formula C₁₄H₁₇NO₃
badge Registry Numbers
MDL Number MFCD17214734
thermostat Physical Properties
Boiling Point 384.5±42.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage -20°C, stored in inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of chiral drugs where the (R)-enantiomer is required for optimal biological activity. Its aldehyde functionality allows for further chemical modifications, such as reductive amination or condensation reactions, enabling the construction of complex nitrogen-containing molecules. Commonly employed in the preparation of bioactive compounds, including protease inhibitors and receptor antagonists. Its protected amine group (via Cbz) facilitates selective reactions at other sites, making it valuable in multi-step organic syntheses, especially in medicinal chemistry and drug discovery.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿3,690.00
(R)-Benzyl 3-formylpiperidine-1-carboxylate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of chiral drugs where the (R)-enantiomer is required for optimal biological activity. Its aldehyde functionality allows for further chemical modifications, such as reductive amination or condensation reactions, enabling the construction of complex nitrogen-containing molecules. Commonly employed in the preparation of bioactive compounds, including protease inhibitors and receptor antagonists. Its protected ami

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of chiral drugs where the (R)-enantiomer is required for optimal biological activity. Its aldehyde functionality allows for further chemical modifications, such as reductive amination or condensation reactions, enabling the construction of complex nitrogen-containing molecules. Commonly employed in the preparation of bioactive compounds, including protease inhibitors and receptor antagonists. Its protected amine group (via Cbz) facilitates selective reactions at other sites, making it valuable in multi-step organic syntheses, especially in medicinal chemistry and drug discovery.

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