3-[(E)-dodec-1-enyl]oxolane-2,5-dione

99%

Reagent Code: #182889
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CAS Number 25377-73-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 266.37 g/mol
Formula C₁₆H₂₆O₃
thermostat Physical Properties
Melting Point ~45 °C
Boiling Point 150 °C
inventory_2 Storage & Handling
Density 1.005 g/mL
Storage Room temperature, dry

description Product Description

Used primarily as a reactive intermediate in organic synthesis, this compound functions as a specialty acylating agent. Its anhydride functionality enables it to form ester and amide bonds under mild conditions, making it valuable in the preparation of functionalized polymers and surface modifications. It is also employed in the development of lipid-based molecules for pharmaceutical applications due to its ability to mimic long-chain fatty acid derivatives. The presence of the vinyl group allows for further chemical transformations, such as cross-metathesis or radical addition, enabling modular construction of complex molecules. Its cyclic anhydride structure readily opens in the presence of nucleophiles, facilitating conjugation with alcohols or amines in bioconjugation strategies or polymer chemistry.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿1,080.00
inventory 100g
10-20 days ฿2,880.00
inventory 500g
10-20 days ฿8,580.00
inventory 2.5kg
10-20 days ฿34,080.00
3-[(E)-dodec-1-enyl]oxolane-2,5-dione
Used primarily as a reactive intermediate in organic synthesis, this compound functions as a specialty acylating agent. Its anhydride functionality enables it to form ester and amide bonds under mild conditions, making it valuable in the preparation of functionalized polymers and surface modifications. It is also employed in the development of lipid-based molecules for pharmaceutical applications due to its ability to mimic long-chain fatty acid derivatives. The presence of the vinyl group allows for further chemical transformations, such as cross-metathesis or radical addition, enabling modular construction of complex molecules. Its cyclic anhydride structure readily opens in the presence of nucleophiles, facilitating conjugation with alcohols or amines in bioconjugation strategies or polymer chemistry.
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