(R)-2-((4-Nitrophenethyl)amino)-1-phenylethanol

98%

Reagent Code: #113390
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CAS Number 223673-34-5

science Other reagents with same CAS 223673-34-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 286.33 g/mol
Formula C₁₆H₁₈N₂O₃
badge Registry Numbers
MDL Number MFCD26407509
thermostat Physical Properties
Boiling Point 472.5±24.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, away from light, stored in an inert gas

description Product Description

This compound is primarily utilized in the field of medicinal chemistry and pharmacology as a chiral intermediate or building block in the synthesis of more complex molecules. Its structure, featuring both aromatic and amino alcohol functional groups, makes it valuable for developing enantioselective drugs, particularly those targeting neurological or cardiovascular systems. The nitro group enhances its reactivity, enabling further chemical modifications to create potential therapeutic agents. Additionally, it may be used in research to study receptor-ligand interactions due to its ability to mimic certain biologically active molecules. Its chiral nature also makes it relevant in asymmetric synthesis, contributing to the production of optically pure pharmaceuticals.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿567.00
inventory 10g
10-20 days ฿1,620.00
inventory 5g
10-20 days ฿1,134.00

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(R)-2-((4-Nitrophenethyl)amino)-1-phenylethanol
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This compound is primarily utilized in the field of medicinal chemistry and pharmacology as a chiral intermediate or building block in the synthesis of more complex molecules. Its structure, featuring both aromatic and amino alcohol functional groups, makes it valuable for developing enantioselective drugs, particularly those targeting neurological or cardiovascular systems. The nitro group enhances its reactivity, enabling further chemical modifications to create potential therapeutic agents. Additional

This compound is primarily utilized in the field of medicinal chemistry and pharmacology as a chiral intermediate or building block in the synthesis of more complex molecules. Its structure, featuring both aromatic and amino alcohol functional groups, makes it valuable for developing enantioselective drugs, particularly those targeting neurological or cardiovascular systems. The nitro group enhances its reactivity, enabling further chemical modifications to create potential therapeutic agents. Additionally, it may be used in research to study receptor-ligand interactions due to its ability to mimic certain biologically active molecules. Its chiral nature also makes it relevant in asymmetric synthesis, contributing to the production of optically pure pharmaceuticals.

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