Science Elevated.

sales@fluoromart.com

0Your Cart$0.00

Cart (0)

No products in the cart.

167951-80-6 | 4-(Trifluoromethyl)-1,3-dioxolan-2-one

$642.00$642.00

Weight:

Purity:

Purchase CAS:167951-80-6,view related peer-reviewed papers,technical documents,similar products,MSDS & more.
4-(Trifluoromethyl)-1,3-dioxolan-2-one (TFMD) is an organic compound with the molecular formula C3H3F3O2. It is a colorless liquid with a boiling point of 101 °C and a melting point of -41 °C. TFMD is a versatile organic building block used in many organic syntheses, as it can be used to form a variety of compounds, in...

sds

SKU:FM124373
Categories: Fluorinated Blocks
HazMat Fast
HazMat Fast
Global Delivery About 12 days
Research Only
Research Only
All products for research only
Compliant Shipping
Compliant Shipping
Comply global express rules
Split Packaging
Split Packaging
Split packaging options free
Easy Relabeling
Easy Relabeling
With easy-to-change labels
Easy Labels

CAS:167951-80-6 | 4-(Trifluoromethyl)-1,3-dioxolan-2-one ,Description

4-(Trifluoromethyl)-1,3-dioxolan-2-one (TFMD) is an organic compound with the molecular formula C3H3F3O2. It is a colorless liquid with a boiling point of 101 °C and a melting point of -41 °C. TFMD is a versatile organic building block used in many organic syntheses, as it can be used to form a variety of compounds, including heterocycles and organofluorides. It is also used in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
 

Scientific Research Applications

 

  • Lithium Battery Materials: The direct fluorination of 1,3-dioxolan-2-one has been successfully carried out, resulting in 4-fluoro-1,3-dioxolan-2-one, which is expected to be an additive for lithium ion secondary batteries. This also includes the development of trifluoromethanesulfonyl fluoride, an intermediate of lithium battery electrolyte (Kobayashi et al., 2003).
  • Organic Synthesis: Research has been conducted on preparing 4-trifluoroethylidene-1,3-dioxolane derivatives using a new stable (trifluoromethyl)ethynylation reagent. This results in various perfluoroalkylated derivatives, demonstrating the versatility of 1,3-dioxolane in organic synthesis (Jeong et al., 2003).
  • Fluoropolymer Synthesis: A study reported the synthesis of 4-Chloro-5-trifluoromethyl-2,2,4-trifluoro-1,3-dioxolane and its subsequent use in preparing high-Tg amorphous fluoropolymers. These fluoropolymers have potential applications in various high-performance materials (Russo & Navarrini, 2004).
  • Chemical Protection of Compounds: The 1,3-dioxolanation of carbonyl compounds has been investigated, leading to the creation of 4-trimethylsilylmethyl-1,3-dioxolanes. These compounds are significant for the selective protection and regeneration of carbonyl compounds in chemical syntheses (Lillie & Avery, 1994).
  • Building Blocks for Aliphatic Compounds: Synthesis of 5-trifluoromethyl-1,3-dioxin-4-ones has been used for the preparation of various trifluoromethylated aliphatic compounds. These compounds serve as versatile building blocks in organic chemistry (Iwaoka et al., 1992).
  • Liquid Crystal Enhancement: The introduction of 1,3-dioxolane as a terminal group in tolane-liquid crystals was found to significantly increase positive dielectric anisotropy and birefringence. This enhances the performance of liquid crystals in display technologies (Chen et al., 2015).

More Information

Product Name :3,3,3-Trifluoropropylene carbonate
CAS No. :167951-80-6Molecular Weight :156.06
MDL No. :MFCD02183522Purity/ Specification : 
Molecular Formula :C4H3F3O3Storage :Inert atmosphere,2-8°C
Boiling Point :-  
GHS Pictogram : 
Signal Word :WarningPrecautionary Statements :P280-P305+P351+P338
UN# :N/AClass :N/A
Hazard Statements :H317-H319Packing Group :N/A

 

download-icon
MS

download-icon
1HNMR

download-icon
CNMR

download-icon
IR1

download-icon
IR2

download-icon
Raman


 

)

Related products