(R)-2-Chloro-1-(4-fluorophenyl)ethanol

≥98%

Reagent Code: #84839
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CAS Number 126534-43-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 174.60 g/mol
Formula C₈H₈ClFO
badge Registry Numbers
MDL Number MFCD08064295
thermostat Physical Properties
Boiling Point 256.6 °C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry, sealed

description Product Description

This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the production of chiral molecules. Its structure, featuring both chloro and fluoro substituents, makes it a valuable building block for creating active pharmaceutical ingredients (APIs) with specific stereochemistry. It is often employed in the development of drugs targeting central nervous system disorders, cardiovascular diseases, and other therapeutic areas. Additionally, its chiral nature allows for the production of enantiomerically pure compounds, which are crucial for enhancing drug efficacy and reducing side effects. The compound is also used in research settings to study the effects of stereochemistry on biological activity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,125.00
inventory 1g
10-20 days ฿2,799.00
inventory 5g
10-20 days ฿10,080.00
(R)-2-Chloro-1-(4-fluorophenyl)ethanol
This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the production of chiral molecules. Its structure, featuring both chloro and fluoro substituents, makes it a valuable building block for creating active pharmaceutical ingredients (APIs) with specific stereochemistry. It is often employed in the development of drugs targeting central nervous system disorders, cardiovascular diseases, and other therapeutic areas. Additionally, its chiral nature allows for the production of enantiomerically pure compounds, which are crucial for enhancing drug efficacy and reducing side effects. The compound is also used in research settings to study the effects of stereochemistry on biological activity.
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