(αR,βR)-α,β-Diphenyl-1-piperidineethanamine

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Reagent Code: #230985
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CAS Number 1262516-53-9

science Other reagents with same CAS 1262516-53-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 281.4152 g/mol
Formula C₁₉H₂₅N₂
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used primarily in the synthesis of pharmaceutical intermediates, this compound serves as a chiral building block in the development of central nervous system agents. Its structural configuration supports the creation of enantiomerically pure compounds, which are critical in the design of selective dopamine and serotonin modulators. It is also employed in the preparation of ligands for asymmetric catalysis, enhancing stereochemical control in complex organic reactions. Due to its amine functionality and conformational rigidity, it finds use in medicinal chemistry for structure-activity relationship studies, particularly in neuropharmacology research.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,980.00

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(αR,βR)-α,β-Diphenyl-1-piperidineethanamine
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Used primarily in the synthesis of pharmaceutical intermediates, this compound serves as a chiral building block in the development of central nervous system agents. Its structural configuration supports the creation of enantiomerically pure compounds, which are critical in the design of selective dopamine and serotonin modulators. It is also employed in the preparation of ligands for asymmetric catalysis, enhancing stereochemical control in complex organic reactions. Due to its amine functionality and c

Used primarily in the synthesis of pharmaceutical intermediates, this compound serves as a chiral building block in the development of central nervous system agents. Its structural configuration supports the creation of enantiomerically pure compounds, which are critical in the design of selective dopamine and serotonin modulators. It is also employed in the preparation of ligands for asymmetric catalysis, enhancing stereochemical control in complex organic reactions. Due to its amine functionality and conformational rigidity, it finds use in medicinal chemistry for structure-activity relationship studies, particularly in neuropharmacology research.

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