2-AMINO-2'-HYDROXY-1 1'-BINAPHTHALENE

97%

Reagent Code: #43821
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CAS Number 134532-03-9

science Other reagents with same CAS 134532-03-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 285.3392 g/mol
Formula C₂₀H₁₅NO
thermostat Physical Properties
Melting Point 195.5-196.5 ℃ (decomp)
Boiling Point 471.5±30.0 ℃(Predicted)
inventory_2 Storage & Handling
Density 1.275±0.06 g/cm3(Predicted)
Storage room temperature

description Product Description

This chemical is primarily used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It is often employed in the formation of chiral catalysts for organic transformations, such as hydrogenation, carbon-carbon bond formation, and oxidation reactions. Its unique structure allows it to effectively induce chirality in the resulting products, making it valuable in the synthesis of pharmaceuticals and fine chemicals. Additionally, it finds application in the development of chiral sensors and materials for optical and electronic devices.

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Test Parameter Specification
Appearance White to Off-White to Light Yellow to Yellow to Light Brown to Brown Powder
Purity (%) 96.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿11,853.00
inventory 250mg
10-20 days ฿981.00
inventory 1g
10-20 days ฿2,376.00

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2-AMINO-2'-HYDROXY-1 1'-BINAPHTHALENE
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This chemical is primarily used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It is often employed in the formation of chiral catalysts for organic transformations, such as hydrogenation, carbon-carbon bond formation, and oxidation reactions. Its unique structure allows it to effectively induce chirality in the resulting products, making it valuable in the synthesis of pharmaceuticals and fine chemicals. Additionally, it finds applica

This chemical is primarily used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It is often employed in the formation of chiral catalysts for organic transformations, such as hydrogenation, carbon-carbon bond formation, and oxidation reactions. Its unique structure allows it to effectively induce chirality in the resulting products, making it valuable in the synthesis of pharmaceuticals and fine chemicals. Additionally, it finds application in the development of chiral sensors and materials for optical and electronic devices.

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