(S)-(-)-1,1,2-Triphenylethane-1,2-diol

97%

Reagent Code: #234710
label
Alias (S)-triphenylethylene glycol; (S)-triphenyl-1,2-ethylene glycol
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CAS Number 108998-83-0

science Other reagents with same CAS 108998-83-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 290.36 g/mol
Formula C₂₀H₁₈O₂
badge Registry Numbers
MDL Number MFCD00075492
thermostat Physical Properties
Melting Point 125-127°C (lit.)
inventory_2 Storage & Handling
Storage Room temperature, sealed

description Product Description

Used as a chiral auxiliary and asymmetric synthesis intermediate in pharmaceutical chemistry. Its rigid, sterically hindered structure makes it valuable for controlling stereochemistry in complex organic reactions. Commonly employed in the development of chiral ligands and catalysts for enantioselective transformations. Also applied in the preparation of optically active compounds, including bioactive molecules and natural products, where high enantiomeric purity is required.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿379.50
inventory 5g
10-20 days ฿1,523.50
inventory 25g
10-20 days ฿10,050.00
(S)-(-)-1,1,2-Triphenylethane-1,2-diol
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Used as a chiral auxiliary and asymmetric synthesis intermediate in pharmaceutical chemistry. Its rigid, sterically hindered structure makes it valuable for controlling stereochemistry in complex organic reactions. Commonly employed in the development of chiral ligands and catalysts for enantioselective transformations. Also applied in the preparation of optically active compounds, including bioactive molecules and natural products, where high enantiomeric purity is required.

Used as a chiral auxiliary and asymmetric synthesis intermediate in pharmaceutical chemistry. Its rigid, sterically hindered structure makes it valuable for controlling stereochemistry in complex organic reactions. Commonly employed in the development of chiral ligands and catalysts for enantioselective transformations. Also applied in the preparation of optically active compounds, including bioactive molecules and natural products, where high enantiomeric purity is required.

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