4-Aminotetrahydropyran

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Reagent Code: #134566
label
Alias 4-aminotetrahydropyran
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CAS Number 38041-19-9

science Other reagents with same CAS 38041-19-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 101.15 g/mol
Formula C₅H₁₁NO
badge Registry Numbers
MDL Number MFCD02179436
thermostat Physical Properties
Boiling Point 60 °C
inventory_2 Storage & Handling
Density 0.977g/cm3at 25℃
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents and kinase inhibitors. Its structure supports the formation of bioactive molecules due to the presence of both amine and ether functional groups, enabling hydrogen bonding and improved solubility. Commonly employed in medicinal chemistry for scaffold modification to enhance metabolic stability and target binding affinity. Also utilized in the preparation of functionalized heterocycles for drug discovery research.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿180.00
inventory 1g
10-20 days ฿390.00
inventory 5g
10-20 days ฿690.00
inventory 25g
10-20 days ฿2,330.00
inventory 100g
10-20 days ฿7,930.00

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4-Aminotetrahydropyran
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents and kinase inhibitors. Its structure supports the formation of bioactive molecules due to the presence of both amine and ether functional groups, enabling hydrogen bonding and improved solubility. Commonly employed in medicinal chemistry for scaffold modification to enhance metabolic stability and target binding affinity. Also utilized in the preparation of functionalized heterocy

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents and kinase inhibitors. Its structure supports the formation of bioactive molecules due to the presence of both amine and ether functional groups, enabling hydrogen bonding and improved solubility. Commonly employed in medicinal chemistry for scaffold modification to enhance metabolic stability and target binding affinity. Also utilized in the preparation of functionalized heterocycles for drug discovery research.

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