(4S,4'S)-4,4'-Di((S)-sec-butyl)-4,4',5,5'-tetrahydro-2,2'-bioxazole

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Reagent Code: #69786
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CAS Number 133463-89-5

science Other reagents with same CAS 133463-89-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 252.35 g/mol
Formula C₁₄H₂₄N₂O₂
badge Registry Numbers
MDL Number MFCD33022379
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored under inert gas

description Product Description

Used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It plays a significant role in the formation of chiral centers in organic molecules, aiding in the production of pharmaceuticals and fine chemicals with high enantiomeric purity. Its application extends to hydrogenation and other transition metal-catalyzed processes, enhancing the efficiency and selectivity of these reactions. Additionally, it is employed in the development of advanced materials and agrochemicals, where precise stereochemical control is essential.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿22,221.00
inventory 100mg
10-20 days ฿3,204.00
inventory 250mg
10-20 days ฿7,074.00

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(4S,4'S)-4,4'-Di((S)-sec-butyl)-4,4',5,5'-tetrahydro-2,2'-bioxazole
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Used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It plays a significant role in the formation of chiral centers in organic molecules, aiding in the production of pharmaceuticals and fine chemicals with high enantiomeric purity. Its application extends to hydrogenation and other transition metal-catalyzed processes, enhancing the efficiency and selectivity of these reactions. Additionally, it is employed in the development of advance

Used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It plays a significant role in the formation of chiral centers in organic molecules, aiding in the production of pharmaceuticals and fine chemicals with high enantiomeric purity. Its application extends to hydrogenation and other transition metal-catalyzed processes, enhancing the efficiency and selectivity of these reactions. Additionally, it is employed in the development of advanced materials and agrochemicals, where precise stereochemical control is essential.

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