(R)-1-(6-Methoxypyridin-2-yl)ethanamine

98%

Reagent Code: #230978
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CAS Number 1212888-81-7

science Other reagents with same CAS 1212888-81-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 152.19 g/mol
Formula C₈H₁₂N₂O
badge Registry Numbers
MDL Number MFCD09824158
thermostat Physical Properties
Boiling Point 223.8±30.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.057±0.06 g/cm3(Predicted)
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of selective kinase inhibitors. It plays an important role in developing drugs for the treatment of inflammatory diseases and certain cancers due to its ability to enhance selectivity and potency of active pharmaceutical ingredients. Its chiral amine structure allows for precise stereochemical control in drug design, improving metabolic stability and reducing off-target effects. Commonly employed in asymmetric synthesis and catalysis in medicinal chemistry research.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,990.00
inventory 250mg
10-20 days ฿4,750.00

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(R)-1-(6-Methoxypyridin-2-yl)ethanamine
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Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of selective kinase inhibitors. It plays an important role in developing drugs for the treatment of inflammatory diseases and certain cancers due to its ability to enhance selectivity and potency of active pharmaceutical ingredients. Its chiral amine structure allows for precise stereochemical control in drug design, improving metabolic stability and reducing off-target effects. Commonly employed in asym

Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of selective kinase inhibitors. It plays an important role in developing drugs for the treatment of inflammatory diseases and certain cancers due to its ability to enhance selectivity and potency of active pharmaceutical ingredients. Its chiral amine structure allows for precise stereochemical control in drug design, improving metabolic stability and reducing off-target effects. Commonly employed in asymmetric synthesis and catalysis in medicinal chemistry research.

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