(1S,2S)-N1,N1,N2,N2-Tetramethyl-1,2-diphenylethane-1,2-diamine

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Reagent Code: #87033
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CAS Number 91361-07-8

science Other reagents with same CAS 91361-07-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 268.40 g/mol
Formula C₁₈H₂₄N₂
badge Registry Numbers
MDL Number MFCD06797770
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored under inert gas

description Product Description

This compound is primarily utilized in asymmetric synthesis and catalysis, particularly in enantioselective reactions. It serves as a chiral ligand in transition metal-catalyzed processes, enabling the production of optically active compounds with high selectivity. Its application is significant in the pharmaceutical industry for the synthesis of chiral drugs, where the precise control of stereochemistry is crucial. Additionally, it is employed in the development of advanced materials and fine chemicals, contributing to the creation of complex molecular architectures with specific stereochemical properties.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿639.00
inventory 100mg
10-20 days ฿1,098.00
inventory 250mg
10-20 days ฿2,079.00

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(1S,2S)-N1,N1,N2,N2-Tetramethyl-1,2-diphenylethane-1,2-diamine
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This compound is primarily utilized in asymmetric synthesis and catalysis, particularly in enantioselective reactions. It serves as a chiral ligand in transition metal-catalyzed processes, enabling the production of optically active compounds with high selectivity. Its application is significant in the pharmaceutical industry for the synthesis of chiral drugs, where the precise control of stereochemistry is crucial. Additionally, it is employed in the development of advanced materials and fine chemicals,

This compound is primarily utilized in asymmetric synthesis and catalysis, particularly in enantioselective reactions. It serves as a chiral ligand in transition metal-catalyzed processes, enabling the production of optically active compounds with high selectivity. Its application is significant in the pharmaceutical industry for the synthesis of chiral drugs, where the precise control of stereochemistry is crucial. Additionally, it is employed in the development of advanced materials and fine chemicals, contributing to the creation of complex molecular architectures with specific stereochemical properties.

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