[S-(R,S)]-()-N-(1-Phenylethyl)-1-Azabicyclo[2.2.2]Octan-3-Amine Dihydrochloride

98%

Reagent Code: #237110
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CAS Number 120570-09-4

science Other reagents with same CAS 120570-09-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 303.27 g/mol
Formula C₁₅H₂₄Cl₂N₂
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used primarily in the pharmaceutical industry as a chiral resolving agent, this compound plays a key role in the separation of enantiomers, particularly in the purification of racemic mixtures of basic drugs. Its rigid bicyclic structure and stereochemical properties make it effective in forming diastereomeric salts with chiral acids, enabling the isolation of single enantiomers with high optical purity. It is especially valuable in the synthesis of active pharmaceutical ingredients where stereochemistry significantly impacts drug efficacy and safety. Additionally, it has been employed in asymmetric synthesis and as a chiral auxiliary in organic reactions to control stereoselectivity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,130.00
[S-(R,S)]-()-N-(1-Phenylethyl)-1-Azabicyclo[2.2.2]Octan-3-Amine Dihydrochloride
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Used primarily in the pharmaceutical industry as a chiral resolving agent, this compound plays a key role in the separation of enantiomers, particularly in the purification of racemic mixtures of basic drugs. Its rigid bicyclic structure and stereochemical properties make it effective in forming diastereomeric salts with chiral acids, enabling the isolation of single enantiomers with high optical purity. It is especially valuable in the synthesis of active pharmaceutical ingredients where stereochemistry

Used primarily in the pharmaceutical industry as a chiral resolving agent, this compound plays a key role in the separation of enantiomers, particularly in the purification of racemic mixtures of basic drugs. Its rigid bicyclic structure and stereochemical properties make it effective in forming diastereomeric salts with chiral acids, enabling the isolation of single enantiomers with high optical purity. It is especially valuable in the synthesis of active pharmaceutical ingredients where stereochemistry significantly impacts drug efficacy and safety. Additionally, it has been employed in asymmetric synthesis and as a chiral auxiliary in organic reactions to control stereoselectivity.

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