6,6'-Bis((S)-4-benzyl-4,5-dihydrooxazol-2-yl)-2,2'-bipyridine

95%

Reagent Code: #49372
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CAS Number 2088982-18-5

science Other reagents with same CAS 2088982-18-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 474.5500 g/mol
Formula C₃₀H₂₆N₄O₂
badge Registry Numbers
MDL Number MFCD00009593
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in enantioselective synthesis. It is highly effective in facilitating asymmetric hydrogenation, a process critical for producing chiral molecules in pharmaceuticals and fine chemicals. Its rigid bipyridine core, combined with chiral oxazoline moieties, allows for precise control over stereochemistry, making it valuable in the synthesis of complex organic compounds with high enantiomeric purity. Additionally, it is employed in the development of advanced materials, such as chiral polymers or metal-organic frameworks, where its structural properties enhance selectivity and functionality. Its application extends to academic research, where it serves as a model ligand for studying asymmetric induction and catalytic mechanisms.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿26,730.00
250mg
10-20 days ฿8,820.00
100mg
10-20 days ฿4,194.00
6,6'-Bis((S)-4-benzyl-4,5-dihydrooxazol-2-yl)-2,2'-bipyridine
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This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in enantioselective synthesis. It is highly effective in facilitating asymmetric hydrogenation, a process critical for producing chiral molecules in pharmaceuticals and fine chemicals. Its rigid bipyridine core, combined with chiral oxazoline moieties, allows for precise control over stereochemistry, making it valuable in the synthesis of complex organic compounds with high enantiomeric purity. Additionally, it i

This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in enantioselective synthesis. It is highly effective in facilitating asymmetric hydrogenation, a process critical for producing chiral molecules in pharmaceuticals and fine chemicals. Its rigid bipyridine core, combined with chiral oxazoline moieties, allows for precise control over stereochemistry, making it valuable in the synthesis of complex organic compounds with high enantiomeric purity. Additionally, it is employed in the development of advanced materials, such as chiral polymers or metal-organic frameworks, where its structural properties enhance selectivity and functionality. Its application extends to academic research, where it serves as a model ligand for studying asymmetric induction and catalytic mechanisms.

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