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

95.0%(GC)

Reagent Code: #158259
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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
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

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 battery performance by improving the stability of the solid electrolyte interphase (SEI) layer. It also serves in the preparation of specialty polymers and as a protecting group reagent in organic synthesis due to its ability to introduce dioxolane functionalities. Its cyclic carbonate structure makes it valuable in reactions requiring controlled release or activation of functional groups.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿4,110.00
inventory 25g
10-20 days ฿12,250.00
inventory 100g
10-20 days ฿36,020.00
inventory 500g
10-20 days ฿108,120.00

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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 battery performance by improving the stability of the solid electrolyte interphase (SEI) layer. It also serves in the preparation of specialty polymers and as a protecting group reagent in organic synthesis due to its ability to introduce dioxolane functionalities. Its cyclic carbonate structure makes it valuable in reactions requiring controlle

Used as a key intermediate in the synthesis of lithium-ion battery electrolytes, particularly in the production of fluoroethylene carbonate (FEC), which enhances battery performance by improving the stability of the solid electrolyte interphase (SEI) layer. It also serves in the preparation of specialty polymers and as a protecting group reagent in organic synthesis due to its ability to introduce dioxolane functionalities. Its cyclic carbonate structure makes it valuable in reactions requiring controlled release or activation of functional groups.

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