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Fluorine battery additives

  • CAS:406-95-1,2,2,2-Trifluoroethyl acetate(TFA)
CAS:406-95-1,2,2,2-Trifluoroethyl acetate(TFA)

CAS:406-95-1,2,2,2-Trifluoroethyl acetate(TFA)

  • Specification:98%
  • Properties:Liquid
  • Package:fluorinated bottle
  • Usage:Lithium battery additives
  • Product description: CAS:406-95-1 | 2,2,2-Trifluoroethyl acetate (TFA), a fluorine-containing lithium battery additive, has the function of film formation and ignition point improvement
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2,2,2-TRIFLUOROETHYL ACETATE Basic information
Product Name: 2,2,2-TRIFLUOROETHYL ACETATE
Synonyms: 2,2,2-TRIFLUOROETHYL ACETATE;Acetic acid 2,2,2-trifluoroethyl ester;2,2,2-Trifluoroethyl acetate 97%;2,2,2-Trifluoroethylacetate97%;2,2,2-Trifluoroethanol acetate;2-Acetoxy-1,1,1-trifluoroethane, 1-(2,2,2-Trifluoroethoxy)ethan-1-one, 2,2,2-Trifluoroethyl ethanoate;2,2,2-Trifluoroethyl ethanoate, Acetic acid 2,2,2-trifluoroethyl ester;Trifluoroethyl acetate
CAS: 406-95-1
MF: C4H5F3O2
MW: 142.08
EINECS: 671-427-3
Product Categories:
Mol File: 406-95-1.mol

2,2,2-TRIFLUOROETHYL ACETATE Chemical Properties
Boiling point 78 °C
density 1,258 g/cm3
refractive index 1.3202
Fp 11°C
Specific Gravity 1.258
Water Solubility Soluble in water (16 g/L) (25°C)
BRN 1757502
CAS DataBase Reference 406-95-1(CAS DataBase Reference)
Safety Information
Hazard Codes F
Risk Statements 11
Safety Statements 16-23-24/25
RIDADR 3272
Hazard Note Flammable
HazardClass 3
PackingGroup III

MSDS Information

FLUORINATED ELECTROLYTE COMPOSITION FOR AN ELECTROCHEMICAL CELL HAVING A LITHIUM OR LITHIUM ALLOY ANODE

Current Patent Assignee: SAFT - US2024/6662, 2024, A1
Patent Family Members: EP4241321 A1; FR3116156 A1; FR3116156 B1; US2024/6662 A1; WO2022/96220 A1

Abstract

The invention relates to an electrochemical cell comprising: —at least one anode comprising metallic lithium or a lithium alloy or at least one anode comprising a current collector at least partially covered with metallic lithium deposited after at least one charge of the cell, the cell not containing metallic lithium at the time of its manufacture, —at least one cathode, - a liquid or gelled electrolyte composition comprising: a) a solvent comprising: i) either a mixture of 1,1,1,3,3,3-hexafluoro-2-methoxypropane (HFMP) and/or 1,1,1,3,3,3-hexafluoro-2-(fluoromethoxy)propane (HFMFP), ethylene monofluorocarbonate (F1EC) and 2,2,2-trifluoroethyl methyl carbonate (F3EMC), ii) or a mixture of 1,1,1,3,3,3-hexafluoro-2-methoxypropane (HFMP) and/or 1,1,1,3,3,3-hexafluo-ro-2-(fluoromethoxy)propane (HFMFP), ethylene monofluorocarbonate (F1EC) and 2,2,2-trifluoroethyl acetate (F3EA), b) at least one salt whose cation is the lithium cation, c) lithium difluorophosphate LiPO2Fin an amount representing from 0.05 to 5% of the mass of the combination made up of the solvent and said at least one dissolved lithium salt.

A bifunctional co-solvent wide-temperature lithium-ion battery electrolyte and its application

Current Patent Assignee: GUIZHOU MEILING POWER SUPPLY CO LTD - CN117352839, 2024, A
Patent Family Members: CN117352839 A


Abstract

The present invention relates to a bifunctional co-solvent wide-temperature lithium-ion battery electrolyte and its application, and the wide-temperature lithium-ion battery electrolyte is composed of lithium salt, organic solvent, thionyl chloride, tris(trimethylsilane) phosphate, additives. The lithium-ion battery prepared by the bifunctional co-solvent wide-temperature electrolyte described in the present invention effectively broadens the range of temperature use, improves the high-temperature cycle performance and low-temperature discharge of the battery, has the characteristics of wide temperature working range, high specific energy and long cycle life, and has excellent thermal stability and good safety performance.

Methods and intermediates used in the preparation of BTK inhibitors

Current Patent Assignee: JANSSEN PHARMACEUTICA NV - CN109790121, 2024, B
Patent Family Members: CN109790121 A; CN109790121 B; EP3523280 A1; JP2019/532959 A; US2020/39981 A1; ...


Abstract

A method for the preparation of certain intermediates (e.g., the following compounds: (I)) is disclosed that can be used to prepare BTK inhibitors, such as ibrutinib.