(S)-Bis((S)-1-(naphthalen-1-yl)ethyl)amine hydrochloride

97%

Reagent Code: #235846
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CAS Number 171867-34-8

science Other reagents with same CAS 171867-34-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 361.91 g/mol
Formula C₂₄H₂₄ClN
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a chiral auxiliary and asymmetric synthesis reagent in pharmaceutical chemistry. Facilitates enantioselective transformations by inducing chirality in reactions such as alkylations, aldol additions, and Michael additions. Commonly employed in the development of optically active drugs where stereochemistry is critical. Its bulky naphthyl groups enhance stereoselectivity, making it valuable in the synthesis of complex natural products and bioactive molecules. Also applied in the preparation of chiral ligands for transition metal-catalyzed asymmetric reactions. Stable under various reaction conditions, it allows for broad utility in multi-step synthetic routes.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿2,730.00
inventory 100mg
10-20 days ฿4,520.00
inventory 250mg
10-20 days ฿9,120.00
(S)-Bis((S)-1-(naphthalen-1-yl)ethyl)amine hydrochloride
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Used as a chiral auxiliary and asymmetric synthesis reagent in pharmaceutical chemistry. Facilitates enantioselective transformations by inducing chirality in reactions such as alkylations, aldol additions, and Michael additions. Commonly employed in the development of optically active drugs where stereochemistry is critical. Its bulky naphthyl groups enhance stereoselectivity, making it valuable in the synthesis of complex natural products and bioactive molecules. Also applied in the preparation of chir

Used as a chiral auxiliary and asymmetric synthesis reagent in pharmaceutical chemistry. Facilitates enantioselective transformations by inducing chirality in reactions such as alkylations, aldol additions, and Michael additions. Commonly employed in the development of optically active drugs where stereochemistry is critical. Its bulky naphthyl groups enhance stereoselectivity, making it valuable in the synthesis of complex natural products and bioactive molecules. Also applied in the preparation of chiral ligands for transition metal-catalyzed asymmetric reactions. Stable under various reaction conditions, it allows for broad utility in multi-step synthetic routes.

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