(S)-N,N’-Dibenzyl-1,1'-binaphthyldiamine

≥98%,≥99%e.e.

Reagent Code: #65672

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 464.6 g/mol
Formula C₃₄H₂₈N₂
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

(S)-N,N’-Dibenzyl-1,1'-binaphthyldiamine is widely used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions. It plays a crucial role in facilitating enantioselective transformations, such as hydrogenation, carbon-carbon bond formation, and other stereospecific reactions. Its application is prominent in the pharmaceutical industry, where it aids in the production of chiral drugs, ensuring high enantiomeric purity. Additionally, it is utilized in academic research for developing novel catalytic systems and studying chiral induction mechanisms. Its robust structure and ability to form stable complexes with transition metals make it a valuable tool in organic synthesis.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,016.00
inventory 500mg
10-20 days ฿41,337.00

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(S)-N,N’-Dibenzyl-1,1'-binaphthyldiamine
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(S)-N,N’-Dibenzyl-1,1'-binaphthyldiamine is widely used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions. It plays a crucial role in facilitating enantioselective transformations, such as hydrogenation, carbon-carbon bond formation, and other stereospecific reactions. Its application is prominent in the pharmaceutical industry, where it aids in the production of chiral drugs, ensuring high enantiomeric purity. Additionally, it is utilized in academic research for developing

(S)-N,N’-Dibenzyl-1,1'-binaphthyldiamine is widely used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions. It plays a crucial role in facilitating enantioselective transformations, such as hydrogenation, carbon-carbon bond formation, and other stereospecific reactions. Its application is prominent in the pharmaceutical industry, where it aids in the production of chiral drugs, ensuring high enantiomeric purity. Additionally, it is utilized in academic research for developing novel catalytic systems and studying chiral induction mechanisms. Its robust structure and ability to form stable complexes with transition metals make it a valuable tool in organic synthesis.

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