4-Chloro-1,3-dioxolan-2-one

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Reagent Code: #159795
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CAS Number 3967-54-2

science Other reagents with same CAS 3967-54-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 122.50 g/mol
Formula C₃H₃ClO₃
badge Registry Numbers
MDL Number MFCD00005383
thermostat Physical Properties
Boiling Point 121-123°C 18mm Hg (Lit.)
inventory_2 Storage & Handling
Storage 2~8°C, sealed

description Product Description

Used as a key intermediate in the synthesis of lithium-ion battery electrolytes, particularly in the production of fluoroethylene carbonate (FEC), which enhances the stability and performance of the solid electrolyte interphase (SEI) layer on silicon-based anodes. Also employed in organic synthesis for introducing the dioxolane ring in pharmaceuticals and agrochemicals due to its reactivity as a cyclic carbonate. Its chloro-substituent allows further functionalization, making it valuable in fine chemical manufacturing.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿560.00
inventory 5g
10-20 days ฿1,290.00
inventory 25g
10-20 days ฿3,990.00
inventory 100g
10-20 days ฿15,260.00

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4-Chloro-1,3-dioxolan-2-one
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Used as a key intermediate in the synthesis of lithium-ion battery electrolytes, particularly in the production of fluoroethylene carbonate (FEC), which enhances the stability and performance of the solid electrolyte interphase (SEI) layer on silicon-based anodes. Also employed in organic synthesis for introducing the dioxolane ring in pharmaceuticals and agrochemicals due to its reactivity as a cyclic carbonate. Its chloro-substituent allows further functionalization, making it valuable in fine chemical

Used as a key intermediate in the synthesis of lithium-ion battery electrolytes, particularly in the production of fluoroethylene carbonate (FEC), which enhances the stability and performance of the solid electrolyte interphase (SEI) layer on silicon-based anodes. Also employed in organic synthesis for introducing the dioxolane ring in pharmaceuticals and agrochemicals due to its reactivity as a cyclic carbonate. Its chloro-substituent allows further functionalization, making it valuable in fine chemical manufacturing.

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