(R)-()-2-Amino-2'-hydroxy-1,1'-binaphthyl

98.0%

Reagent Code: #60199
label
Alias (R)-NOBIN (R)-(+)-2′-amino-1,1′-binaphth-2-ol (R)-(+)-1-(2-Amino-1-naphthyl)-2-naphthol
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CAS Number 137848-28-3

science Other reagents with same CAS 137848-28-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 285.34 g/mol
Formula C₂₀H₁₅NO
badge Registry Numbers
MDL Number MFCD01882346
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This chemical is primarily utilized 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, oxidation, and carbon-carbon bond-forming reactions. Its ability to induce high enantiomeric excess makes it valuable in the production of pharmaceuticals and fine chemicals, where specific stereochemistry is essential for biological activity. Additionally, it finds application in the development of chiral sensors and materials for enantiomeric recognition and separation processes.

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Test Parameter Specification
Melting point 171-175
Purity (HPLC) 98-100%
Purity (Non-Aqueous Titration) 97-100%
Specific Rotation [α]_D^{20} (THF) 117-123
Appearance White solid

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,380.00
inventory 500mg
10-20 days ฿16,460.00
inventory 1g
10-20 days ฿26,370.00

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(R)-()-2-Amino-2'-hydroxy-1,1'-binaphthyl
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This chemical is primarily utilized 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, oxidation, and carbon-carbon bond-forming reactions. Its ability to induce high enantiomeric excess makes it valuable in the production of pharmaceuticals and fine chemicals, where specific stereochemistry is essential for biological activity. Ad

This chemical is primarily utilized 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, oxidation, and carbon-carbon bond-forming reactions. Its ability to induce high enantiomeric excess makes it valuable in the production of pharmaceuticals and fine chemicals, where specific stereochemistry is essential for biological activity. Additionally, it finds application in the development of chiral sensors and materials for enantiomeric recognition and separation processes.

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