1,1,2,2-Tetraphenyl-1,2-ethanediol

95%

Reagent Code: #242120
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CAS Number 464-72-2

science Other reagents with same CAS 464-72-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 366.45 g/mol
Formula C₂₆H₂₂O₂
badge Registry Numbers
MDL Number MFCD00004448
thermostat Physical Properties
Melting Point 171-173°C (Lit.)
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a chiral ligand or building block in asymmetric synthesis, enabling the formation of stereoselective compounds in pharmaceutical and fine chemical manufacturing. Its rigid, sterically hindered structure makes it valuable in catalysis, particularly in reactions requiring precise spatial control, such as enantioselective reductions or cyclizations. Also employed in the development of optically active materials and as a precursor in the synthesis of complex organic molecules where stereochemistry is critical.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿300.00
inventory 25g
10-20 days ฿420.00
inventory 100g
10-20 days ฿990.00
inventory 500g
10-20 days ฿4,220.00

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1,1,2,2-Tetraphenyl-1,2-ethanediol
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Used as a chiral ligand or building block in asymmetric synthesis, enabling the formation of stereoselective compounds in pharmaceutical and fine chemical manufacturing. Its rigid, sterically hindered structure makes it valuable in catalysis, particularly in reactions requiring precise spatial control, such as enantioselective reductions or cyclizations. Also employed in the development of optically active materials and as a precursor in the synthesis of complex organic molecules where stereochemistry is

Used as a chiral ligand or building block in asymmetric synthesis, enabling the formation of stereoselective compounds in pharmaceutical and fine chemical manufacturing. Its rigid, sterically hindered structure makes it valuable in catalysis, particularly in reactions requiring precise spatial control, such as enantioselective reductions or cyclizations. Also employed in the development of optically active materials and as a precursor in the synthesis of complex organic molecules where stereochemistry is critical.

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