N-(Furan-2-ylmethyl)-N-methylprop-2-en-1-amine

≥95%(stabilized with TBC)

Reagent Code: #214675
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CAS Number 120153-60-8

science Other reagents with same CAS 120153-60-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 151.21 g/mol
Formula C₉H₁₃NO
thermostat Physical Properties
Boiling Point 173.3±20.0 °C(Predicted)
inventory_2 Storage & Handling
Density 0.963±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used primarily as a chemical intermediate in organic synthesis, this compound serves in the development of pharmaceuticals and agrochemicals due to its reactive amine and furan functionalities. Its structure allows for further functionalization, making it useful in constructing nitrogen-containing heterocycles. It is also employed in the preparation of specialty monomers for polymer chemistry, where the allyl group enables cross-linking reactions. Additionally, it has been explored in the design of bioactive molecules, including potential antimicrobial or antifungal agents, leveraging the furan ring’s known biological activity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,820.00
inventory 1g
10-20 days ฿44,980.00
N-(Furan-2-ylmethyl)-N-methylprop-2-en-1-amine
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Used primarily as a chemical intermediate in organic synthesis, this compound serves in the development of pharmaceuticals and agrochemicals due to its reactive amine and furan functionalities. Its structure allows for further functionalization, making it useful in constructing nitrogen-containing heterocycles. It is also employed in the preparation of specialty monomers for polymer chemistry, where the allyl group enables cross-linking reactions. Additionally, it has been explored in the design of bioac

Used primarily as a chemical intermediate in organic synthesis, this compound serves in the development of pharmaceuticals and agrochemicals due to its reactive amine and furan functionalities. Its structure allows for further functionalization, making it useful in constructing nitrogen-containing heterocycles. It is also employed in the preparation of specialty monomers for polymer chemistry, where the allyl group enables cross-linking reactions. Additionally, it has been explored in the design of bioactive molecules, including potential antimicrobial or antifungal agents, leveraging the furan ring’s known biological activity.

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