(-)-4,5-Bis[hydroxy(diphenyl)methyl]-2,2-dimethyl-1,3-dioxolane

97.0%

Reagent Code: #70778
label
Alias (-)-2,3-O-Isopropylidene-1,1,4,4-tetraphenyl-L-threitol (4R,5R)-4,5-bis(diphenylhydroxymethyl)-2,2-dimethyldioxolane 1,1,4,4-Tetraphenyl-2,3-O-isopropylidene-L-threitol TADDOL
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CAS Number 93379-48-7

science Other reagents with same CAS 93379-48-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 466.58 g/mol
Formula C₃₁H₃₀O₄
badge Registry Numbers
MDL Number MFCD00064467
thermostat Physical Properties
Melting Point 193-195 °C(lit.)
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This compound is primarily utilized in the field of asymmetric synthesis, where it serves as a chiral auxiliary or ligand. Its structure, featuring two hydroxy(diphenyl)methyl groups, makes it effective in inducing chirality in chemical reactions, particularly in the formation of enantiomerically pure products. It is often employed in catalytic processes, such as asymmetric hydrogenation and carbon-carbon bond-forming reactions, where high enantioselectivity is crucial. Additionally, its stability and steric properties make it suitable for use in organometallic chemistry, aiding in the development of novel catalysts for pharmaceutical and fine chemical synthesis.

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Test Parameter Specification
Appearance White solid
Purity 97
Specific Rotation (A20/D, C1, CHCl3) -71 to -62
Melting Point 194-198

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿570.00
inventory 5g
10-20 days ฿2,100.00
inventory 25g
10-20 days ฿9,080.00

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(-)-4,5-Bis[hydroxy(diphenyl)methyl]-2,2-dimethyl-1,3-dioxolane
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This compound is primarily utilized in the field of asymmetric synthesis, where it serves as a chiral auxiliary or ligand. Its structure, featuring two hydroxy(diphenyl)methyl groups, makes it effective in inducing chirality in chemical reactions, particularly in the formation of enantiomerically pure products. It is often employed in catalytic processes, such as asymmetric hydrogenation and carbon-carbon bond-forming reactions, where high enantioselectivity is crucial. Additionally, its stability and st

This compound is primarily utilized in the field of asymmetric synthesis, where it serves as a chiral auxiliary or ligand. Its structure, featuring two hydroxy(diphenyl)methyl groups, makes it effective in inducing chirality in chemical reactions, particularly in the formation of enantiomerically pure products. It is often employed in catalytic processes, such as asymmetric hydrogenation and carbon-carbon bond-forming reactions, where high enantioselectivity is crucial. Additionally, its stability and steric properties make it suitable for use in organometallic chemistry, aiding in the development of novel catalysts for pharmaceutical and fine chemical synthesis.

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