(S)-5,5',6,6',7,7',8,8'-Octahydro-[1,1'-binaphthalene]-2,2'-diamine

≥98%

Reagent Code: #38551
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CAS Number 229177-78-0

science Other reagents with same CAS 229177-78-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 292 g/mol
Formula C₂₀H₂₄N₂
inventory_2 Storage & Handling
Density 1.156
Storage room temperature

description Product Description

This chemical is primarily utilized in asymmetric synthesis and catalysis, particularly in the development of chiral ligands for transition metal complexes. It is employed in enantioselective reactions, such as hydrogenation, carbon-carbon bond formation, and other transformations where high stereochemical control is required. The compound's rigid binaphthalene backbone and chiral diamine functionality make it effective in inducing chirality in products, which is crucial in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. Additionally, it serves as a building block for designing advanced materials and catalysts with specific stereochemical properties.

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Test Parameter Specification
Appearance Light Brown Powder
Purity 98-100
Infrared Spectrum Conforms to Structure

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿66,880.00
inventory 250mg
10-20 days ฿6,680.00
inventory 1g
10-20 days ฿19,800.00

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(S)-5,5',6,6',7,7',8,8'-Octahydro-[1,1'-binaphthalene]-2,2'-diamine
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This chemical is primarily utilized in asymmetric synthesis and catalysis, particularly in the development of chiral ligands for transition metal complexes. It is employed in enantioselective reactions, such as hydrogenation, carbon-carbon bond formation, and other transformations where high stereochemical control is required. The compound's rigid binaphthalene backbone and chiral diamine functionality make it effective in inducing chirality in products, which is crucial in the synthesis of pharmaceutica

This chemical is primarily utilized in asymmetric synthesis and catalysis, particularly in the development of chiral ligands for transition metal complexes. It is employed in enantioselective reactions, such as hydrogenation, carbon-carbon bond formation, and other transformations where high stereochemical control is required. The compound's rigid binaphthalene backbone and chiral diamine functionality make it effective in inducing chirality in products, which is crucial in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. Additionally, it serves as a building block for designing advanced materials and catalysts with specific stereochemical properties.

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