(R)-1-(Pyridin-4-yl)ethanol

98%

Reagent Code: #74258
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CAS Number 27854-88-2

science Other reagents with same CAS 27854-88-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 123.15 g/mol
Formula C₇H₉NO
badge Registry Numbers
MDL Number MFCD00077865
thermostat Physical Properties
Melting Point 67-69°C
Boiling Point 239.7°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in the pharmaceutical industry as a chiral building block for the synthesis of various active pharmaceutical ingredients (APIs). Its chiral nature makes it valuable in the production of enantiomerically pure drugs, which are crucial for ensuring efficacy and reducing side effects. It is often employed in the development of medications targeting neurological disorders, where stereochemistry plays a significant role in drug activity. Additionally, it serves as an intermediate in organic synthesis, particularly in the preparation of complex molecules with specific stereochemical requirements. Its application extends to research settings, where it is used to study chiral catalysis and asymmetric synthesis processes.

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Test Parameter Specification
Appearance White to Yellow Solid
Purity 97.5
Melting Point 65-70
1 Chloroform 53-59

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿750.00
inventory 250mg
10-20 days ฿1,250.00
inventory 1g
10-20 days ฿2,870.00
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(R)-1-(Pyridin-4-yl)ethanol
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This compound is primarily utilized in the pharmaceutical industry as a chiral building block for the synthesis of various active pharmaceutical ingredients (APIs). Its chiral nature makes it valuable in the production of enantiomerically pure drugs, which are crucial for ensuring efficacy and reducing side effects. It is often employed in the development of medications targeting neurological disorders, where stereochemistry plays a significant role in drug activity. Additionally, it serves as an intermediate in organic synthesis, particularly in the preparation of complex molecules with specific stereochemical requirements. Its application extends to research settings, where it is used to study chiral catalysis and asymmetric synthesis processes.
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