(1R,1'R)-1,1'-(Pyridine-2,6-diyl)bis(ethan-1-ol)

95%

Reagent Code: #229132
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CAS Number 143329-86-6

science Other reagents with same CAS 143329-86-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 167.21 g/mol
Formula C₉H₁₃NO₂
badge Registry Numbers
MDL Number MFCD18836929
thermostat Physical Properties
Boiling Point 284.0±30.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.154±0.06 g/cm3(Predicted)
Storage Room temperature, inert gas

description Product Description

Used as a chiral building block in asymmetric synthesis, particularly in the preparation of enantiomerically pure pharmaceuticals and catalysts. Its rigid pyridine core and hydroxyl groups allow for selective functionalization and coordination to metal centers, making it valuable in the design of homogeneous catalysts for stereoselective transformations. Also employed in the synthesis of supramolecular structures and ligands for enantioselective recognition processes.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿40,000.00
inventory 250mg
10-20 days ฿64,000.00
inventory 500mg
10-20 days ฿115,200.00
(1R,1'R)-1,1'-(Pyridine-2,6-diyl)bis(ethan-1-ol)
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Used as a chiral building block in asymmetric synthesis, particularly in the preparation of enantiomerically pure pharmaceuticals and catalysts. Its rigid pyridine core and hydroxyl groups allow for selective functionalization and coordination to metal centers, making it valuable in the design of homogeneous catalysts for stereoselective transformations. Also employed in the synthesis of supramolecular structures and ligands for enantioselective recognition processes.

Used as a chiral building block in asymmetric synthesis, particularly in the preparation of enantiomerically pure pharmaceuticals and catalysts. Its rigid pyridine core and hydroxyl groups allow for selective functionalization and coordination to metal centers, making it valuable in the design of homogeneous catalysts for stereoselective transformations. Also employed in the synthesis of supramolecular structures and ligands for enantioselective recognition processes.

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