(R)-2,2'-Dimethyl-1,1'-binaphthyl

≥98%

Reagent Code: #70289
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CAS Number 19634-89-0

science Other reagents with same CAS 19634-89-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 282.39 g/mol
Formula C₂₂H₁₈
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MDL Number MFCD00048075
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This compound is widely used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It is often employed in transition metal-catalyzed processes, such as hydrogenation, carbon-carbon bond formation, and oxidation reactions, to produce chiral molecules with high enantiomeric purity. Its rigid binaphthyl structure provides excellent steric and electronic control, making it a valuable tool in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. Additionally, it serves as a key component in chiral catalysts and reagents, enabling the production of optically active compounds in industrial and academic research settings.

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Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿7,182.00

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(R)-2,2'-Dimethyl-1,1'-binaphthyl
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This compound is widely used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It is often employed in transition metal-catalyzed processes, such as hydrogenation, carbon-carbon bond formation, and oxidation reactions, to produce chiral molecules with high enantiomeric purity. Its rigid binaphthyl structure provides excellent steric and electronic control, making it a valuable tool in the synthesis of pharmaceuticals, agrochemicals, and f

This compound is widely used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It is often employed in transition metal-catalyzed processes, such as hydrogenation, carbon-carbon bond formation, and oxidation reactions, to produce chiral molecules with high enantiomeric purity. Its rigid binaphthyl structure provides excellent steric and electronic control, making it a valuable tool in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. Additionally, it serves as a key component in chiral catalysts and reagents, enabling the production of optically active compounds in industrial and academic research settings.

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