(R,R)-()-1,2-Diphenyl-1,2-ethanediol

98%

Reagent Code: #229961
label
Alias (R,R)-(+)-1,2-diben-1,2-ethylene glycol; (R,R)-(+)-hydrogenated benzyl
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CAS Number 52340-78-0

science Other reagents with same CAS 52340-78-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 214.26 g/mol
Formula C₁₄H₁₄O₂
badge Registry Numbers
MDL Number MFCD00064254
thermostat Physical Properties
Melting Point 146-149°C (lit.)
inventory_2 Storage & Handling
Storage Room temperature, sealed

description Product Description

Used as a chiral building block in asymmetric synthesis, particularly in the preparation of chiral ligands and catalysts. Its rigid diol structure makes it valuable in the development of enantioselective catalysts for organic transformations such as epoxidations, aldol reactions, and hydrogenations. Also employed in the synthesis of pharmaceuticals and natural products where stereochemical control is critical. Its ability to form stable complexes with metals enhances its utility in coordination chemistry and catalytic systems.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿850.00
5g
10-20 days ฿3,600.00
25g
10-20 days ฿15,050.00
(R,R)-()-1,2-Diphenyl-1,2-ethanediol
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Used as a chiral building block in asymmetric synthesis, particularly in the preparation of chiral ligands and catalysts. Its rigid diol structure makes it valuable in the development of enantioselective catalysts for organic transformations such as epoxidations, aldol reactions, and hydrogenations. Also employed in the synthesis of pharmaceuticals and natural products where stereochemical control is critical. Its ability to form stable complexes with metals enhances its utility in coordination chemistry

Used as a chiral building block in asymmetric synthesis, particularly in the preparation of chiral ligands and catalysts. Its rigid diol structure makes it valuable in the development of enantioselective catalysts for organic transformations such as epoxidations, aldol reactions, and hydrogenations. Also employed in the synthesis of pharmaceuticals and natural products where stereochemical control is critical. Its ability to form stable complexes with metals enhances its utility in coordination chemistry and catalytic systems.

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