(DHQ)2PHAL

95%

Reagent Code: #62468
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CAS Number 140924-50-1

science Other reagents with same CAS 140924-50-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 778.98 g/mol
Formula C₄₈H₅₄N₆O₄
badge Registry Numbers
MDL Number MFCD00191975
thermostat Physical Properties
Melting Point 178 °C (dec.)(lit.)
inventory_2 Storage & Handling
Storage room temperature

description Product Description

(DHQ)2PHAL is widely used as a chiral ligand in asymmetric synthesis, particularly in enantioselective reactions. It plays a crucial role in catalyzing transformations such as the Sharpless asymmetric dihydroxylation, which converts alkenes into chiral diols with high enantioselectivity. This makes it valuable in the pharmaceutical industry for synthesizing enantiomerically pure compounds, which are essential for developing drugs with specific biological activities. Additionally, it is employed in academic research to explore new methodologies for creating complex chiral molecules, contributing to advancements in organic chemistry and material science.

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Test Parameter Specification
Purity (HPLC) 95-100
A20 DC1 Methanol 333-338

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 500mg
10-20 days ฿790.00
inventory 1g
10-20 days ฿1,350.00
inventory 5g
10-20 days ฿5,550.00

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(DHQ)2PHAL
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(DHQ)2PHAL is widely used as a chiral ligand in asymmetric synthesis, particularly in enantioselective reactions. It plays a crucial role in catalyzing transformations such as the Sharpless asymmetric dihydroxylation, which converts alkenes into chiral diols with high enantioselectivity. This makes it valuable in the pharmaceutical industry for synthesizing enantiomerically pure compounds, which are essential for developing drugs with specific biological activities. Additionally, it is employed in academ

(DHQ)2PHAL is widely used as a chiral ligand in asymmetric synthesis, particularly in enantioselective reactions. It plays a crucial role in catalyzing transformations such as the Sharpless asymmetric dihydroxylation, which converts alkenes into chiral diols with high enantioselectivity. This makes it valuable in the pharmaceutical industry for synthesizing enantiomerically pure compounds, which are essential for developing drugs with specific biological activities. Additionally, it is employed in academic research to explore new methodologies for creating complex chiral molecules, contributing to advancements in organic chemistry and material science.

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