(R)-2-Amino-2-(phenanthren-9-yl)ethan-1-ol

95%

Reagent Code: #229349
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CAS Number 1212946-34-3

science Other reagents with same CAS 1212946-34-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 237.3 g/mol
Formula C₁₆H₁₅NO
badge Registry Numbers
MDL Number MFCD09253598
thermostat Physical Properties
Boiling Point 487.4±25.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.233±0.06 g/cm3(Predicted)
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a chiral building block in the synthesis of pharmaceutical intermediates, particularly in the development of asymmetric catalysts and bioactive molecules. Its rigid phenanthryl group enhances stereoselectivity in reactions, making it valuable in enantioselective synthesis. Also employed in the preparation of ligands for transition metal-catalyzed reactions, improving yield and optical purity in drug manufacturing processes. Shows potential in the design of fluorescent probes due to the inherent fluorescence of the phenanthrene moiety, useful in biochemical imaging and sensor applications.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿21,840.00
inventory 250mg
10-20 days ฿32,680.00
inventory 1g
10-20 days ฿81,620.00
(R)-2-Amino-2-(phenanthren-9-yl)ethan-1-ol
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Used as a chiral building block in the synthesis of pharmaceutical intermediates, particularly in the development of asymmetric catalysts and bioactive molecules. Its rigid phenanthryl group enhances stereoselectivity in reactions, making it valuable in enantioselective synthesis. Also employed in the preparation of ligands for transition metal-catalyzed reactions, improving yield and optical purity in drug manufacturing processes. Shows potential in the design of fluorescent probes due to the inherent f

Used as a chiral building block in the synthesis of pharmaceutical intermediates, particularly in the development of asymmetric catalysts and bioactive molecules. Its rigid phenanthryl group enhances stereoselectivity in reactions, making it valuable in enantioselective synthesis. Also employed in the preparation of ligands for transition metal-catalyzed reactions, improving yield and optical purity in drug manufacturing processes. Shows potential in the design of fluorescent probes due to the inherent fluorescence of the phenanthrene moiety, useful in biochemical imaging and sensor applications.

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