(1S,2S)-2-Amino-1,2-diphenylethanol

99%

Reagent Code: #126363
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CAS Number 23190-17-2

science Other reagents with same CAS 23190-17-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 213.28 g/mol
Formula C14H15NO
badge Registry Numbers
MDL Number MFCD03093886
thermostat Physical Properties
Melting Point 116 - 119 ℃
Boiling Point 374.3 ℃ at 760 mmHg
inventory_2 Storage & Handling
Density 1.148±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

This compound is primarily utilized in the synthesis of chiral catalysts and ligands, which are essential in asymmetric synthesis for producing enantiomerically pure pharmaceuticals. It serves as a key intermediate in the preparation of various biologically active molecules, particularly in the development of drugs targeting neurological disorders and cardiovascular diseases. Additionally, it is employed in organic chemistry research to study stereoselective reactions and to develop novel methodologies for constructing complex molecular architectures. Its chiral nature makes it valuable in the production of fine chemicals and agrochemicals where specific stereochemistry is crucial for activity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,470.00
inventory 250mg
10-20 days ฿4,230.00
inventory 1g
10-20 days ฿12,960.00

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(1S,2S)-2-Amino-1,2-diphenylethanol
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This compound is primarily utilized in the synthesis of chiral catalysts and ligands, which are essential in asymmetric synthesis for producing enantiomerically pure pharmaceuticals. It serves as a key intermediate in the preparation of various biologically active molecules, particularly in the development of drugs targeting neurological disorders and cardiovascular diseases. Additionally, it is employed in organic chemistry research to study stereoselective reactions and to develop novel methodologies f

This compound is primarily utilized in the synthesis of chiral catalysts and ligands, which are essential in asymmetric synthesis for producing enantiomerically pure pharmaceuticals. It serves as a key intermediate in the preparation of various biologically active molecules, particularly in the development of drugs targeting neurological disorders and cardiovascular diseases. Additionally, it is employed in organic chemistry research to study stereoselective reactions and to develop novel methodologies for constructing complex molecular architectures. Its chiral nature makes it valuable in the production of fine chemicals and agrochemicals where specific stereochemistry is crucial for activity.

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