4-(Ethoxymethylene)-2-phenyl-2-oxazoline-5-one

98%

Reagent Code: #183834
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CAS Number 15646-46-5

science Other reagents with same CAS 15646-46-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 217.2206 g/mol
Formula C₁₂H₁₁NO₃
badge Registry Numbers
MDL Number MFCD00003204
thermostat Physical Properties
Melting Point 94-96 ℃(dec.)(lit.)
Boiling Point 308.8 ℃ at 760mmHg
inventory_2 Storage & Handling
Density 1.18 g/ml
Storage 2-8℃

description Product Description

Used as a key intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It serves as a heterocyclic building block for constructing complex molecules due to its reactive oxazoline core and electrophilic exocyclic double bond. Commonly employed in cycloaddition reactions and nucleophilic ring-opening processes to form functionalized amides and esters. Its ethoxymethylene group allows for further derivatization, making it valuable in the development of bioactive compounds and specialty polymers.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿2,390.00
inventory 5g
10-20 days ฿7,980.00
inventory 25g
10-20 days ฿28,200.00
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4-(Ethoxymethylene)-2-phenyl-2-oxazoline-5-one
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Used as a key intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It serves as a heterocyclic building block for constructing complex molecules due to its reactive oxazoline core and electrophilic exocyclic double bond. Commonly employed in cycloaddition reactions and nucleophilic ring-opening processes to form functionalized amides and esters. Its ethoxymethylene group allows for further derivatization, making it valuable in the development of bioacti

Used as a key intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It serves as a heterocyclic building block for constructing complex molecules due to its reactive oxazoline core and electrophilic exocyclic double bond. Commonly employed in cycloaddition reactions and nucleophilic ring-opening processes to form functionalized amides and esters. Its ethoxymethylene group allows for further derivatization, making it valuable in the development of bioactive compounds and specialty polymers.

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