(4S,4'S)-2,2'-[2-Phenyl-1-(phenylmethyl)ethylidene]bis[4-(1-methylethyl)-4,5-dihydrooxazole]

≥95%,99%e.e.

Reagent Code: #59726
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CAS Number 444575-98-8

science Other reagents with same CAS 444575-98-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 418.6 g/mol
Formula C₂₇H₃₄N₂O₂
thermostat Physical Properties
Boiling Point 537.2±50.0 °C
inventory_2 Storage & Handling
Density 1.10±0.1 g/mL
Storage room temperature, dry

description Product Description

This chemical is primarily utilized in asymmetric synthesis as a chiral ligand or catalyst. It plays a significant role in facilitating enantioselective reactions, particularly in the formation of chiral centers in organic molecules. Its application is crucial in the pharmaceutical industry, where it helps produce optically active compounds with high stereochemical purity. Additionally, it is employed in the synthesis of complex natural products and fine chemicals, enhancing the efficiency and selectivity of catalytic processes. Its robust structure and chiral properties make it a valuable tool in advancing synthetic methodologies.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿981.00
inventory 250mg
10-20 days ฿1,188.00
inventory 1g
10-20 days ฿2,133.00
inventory 5g
10-20 days ฿10,539.00

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(4S,4'S)-2,2'-[2-Phenyl-1-(phenylmethyl)ethylidene]bis[4-(1-methylethyl)-4,5-dihydrooxazole]
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This chemical is primarily utilized in asymmetric synthesis as a chiral ligand or catalyst. It plays a significant role in facilitating enantioselective reactions, particularly in the formation of chiral centers in organic molecules. Its application is crucial in the pharmaceutical industry, where it helps produce optically active compounds with high stereochemical purity. Additionally, it is employed in the synthesis of complex natural products and fine chemicals, enhancing the efficiency and selectivit

This chemical is primarily utilized in asymmetric synthesis as a chiral ligand or catalyst. It plays a significant role in facilitating enantioselective reactions, particularly in the formation of chiral centers in organic molecules. Its application is crucial in the pharmaceutical industry, where it helps produce optically active compounds with high stereochemical purity. Additionally, it is employed in the synthesis of complex natural products and fine chemicals, enhancing the efficiency and selectivity of catalytic processes. Its robust structure and chiral properties make it a valuable tool in advancing synthetic methodologies.

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