1,2-Diphenylethane-1,2-diol

98%

Reagent Code: #176510
label
Alias Hydrogenated benzoin
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CAS Number 492-70-6

science Other reagents with same CAS 492-70-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 214.26 g/mol
Formula C₁₄H₁₄O₂
badge Registry Numbers
MDL Number MFCD00136059
thermostat Physical Properties
Melting Point 132-135 °C
Boiling Point 373 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.193 g/cm3
Storage Room temperature

description Product Description

Used as a key intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. Its symmetrical diol structure allows for selective transformations, such as ring-forming reactions or protection/deprotection strategies in multi-step syntheses. Commonly employed in the development of ligands for asymmetric catalysis, contributing to the production of chiral molecules. Also utilized in the synthesis of dyes and fluorescent compounds due to its aromatic content and ability to undergo dehydration to form stilbene derivatives. Its reactivity makes it valuable in academic and industrial research for building complex molecular architectures.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,770.00
inventory 1g
10-20 days ฿6,840.00
inventory 5g
10-20 days ฿25,200.00
inventory 10g
10-20 days ฿41,550.00
inventory 25g
10-20 days ฿97,000.00

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1,2-Diphenylethane-1,2-diol
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Used as a key intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. Its symmetrical diol structure allows for selective transformations, such as ring-forming reactions or protection/deprotection strategies in multi-step syntheses. Commonly employed in the development of ligands for asymmetric catalysis, contributing to the production of chiral molecules. Also utilized in the synthesis of dyes and fluorescent compounds due to its aromatic content and abi

Used as a key intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. Its symmetrical diol structure allows for selective transformations, such as ring-forming reactions or protection/deprotection strategies in multi-step syntheses. Commonly employed in the development of ligands for asymmetric catalysis, contributing to the production of chiral molecules. Also utilized in the synthesis of dyes and fluorescent compounds due to its aromatic content and ability to undergo dehydration to form stilbene derivatives. Its reactivity makes it valuable in academic and industrial research for building complex molecular architectures.

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