(R)-2-Benzylpiperidine

98%

Reagent Code: #229542
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CAS Number 203452-46-4

science Other reagents with same CAS 203452-46-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 175.27 g/mol
Formula C₁₂H₁₇N
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MDL Number MFCD20663986
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents. Its structural motif appears in compounds with neuroactive properties, including those targeting dopamine and serotonin receptors. Commonly employed in the preparation of optically active intermediates for drug discovery programs, especially in the design of enzyme inhibitors and receptor modulators. Also utilized in asymmetric synthesis due to its stereochemical stability and ability to direct enantioselective transformations.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿27,840.00

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(R)-2-Benzylpiperidine
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents. Its structural motif appears in compounds with neuroactive properties, including those targeting dopamine and serotonin receptors. Commonly employed in the preparation of optically active intermediates for drug discovery programs, especially in the design of enzyme inhibitors and receptor modulators. Also utilized in asymmetric synthesis due to its stereochemical stabilit

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents. Its structural motif appears in compounds with neuroactive properties, including those targeting dopamine and serotonin receptors. Commonly employed in the preparation of optically active intermediates for drug discovery programs, especially in the design of enzyme inhibitors and receptor modulators. Also utilized in asymmetric synthesis due to its stereochemical stability and ability to direct enantioselective transformations.

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