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433-53-4

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433-53-4 Usage

Description

METHYL DIFLUOROACETATE, also known as MFA, is a colorless liquid with specific chemical properties that make it suitable for various applications across different industries. It is known for its ability to improve thermal stability and inhibit corrosion, making it a valuable compound in the development of advanced technologies.

Uses

Used in Energy Storage Industry:
METHYL DIFLUOROACETATE is used as an electrolyte additive for enhancing the thermal stability of Li-ion batteries. Its application reason is to improve the safety and performance of these batteries, which are widely used in various electronic devices and electric vehicles.
Used in Corrosion Inhibition:
METHYL DIFLUOROACETATE is used as a corrosion inhibitor for the aluminum cathode current collector in lithium-ion cells. The application reason is to prevent the degradation of the cathode material, which can lead to reduced battery performance and a shorter lifespan.

Check Digit Verification of cas no

The CAS Registry Mumber 433-53-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,3 and 3 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 433-53:
(5*4)+(4*3)+(3*3)+(2*5)+(1*3)=54
54 % 10 = 4
So 433-53-4 is a valid CAS Registry Number.
InChI:InChI=1/C3HF5/c4-1(2(5)6)3(7)8/h2H

433-53-4 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • TCI America

  • (M2021)  Methyl Difluoroacetate  >97.0%(GC)

  • 433-53-4

  • 5g

  • 420.00CNY

  • Detail
  • TCI America

  • (M2021)  Methyl Difluoroacetate  >97.0%(GC)

  • 433-53-4

  • 25g

  • 1,580.00CNY

  • Detail
  • Alfa Aesar

  • (B22197)  Methyl difluoroacetate, 98%   

  • 433-53-4

  • 1g

  • 378.0CNY

  • Detail
  • Alfa Aesar

  • (B22197)  Methyl difluoroacetate, 98%   

  • 433-53-4

  • 5g

  • 438.0CNY

  • Detail
  • Alfa Aesar

  • (B22197)  Methyl difluoroacetate, 98%   

  • 433-53-4

  • 25g

  • 1613.0CNY

  • Detail
  • Aldrich

  • (295914)  Methyldifluoroacetate  96%

  • 433-53-4

  • 295914-5G

  • 760.50CNY

  • Detail
  • Aldrich

  • (295914)  Methyldifluoroacetate  96%

  • 433-53-4

  • 295914-25G

  • 2,626.65CNY

  • Detail

433-53-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name METHYL DIFLUOROACETATE

1.2 Other means of identification

Product number -
Other names Difluoroacetic Acid Methyl Ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:433-53-4 SDS

433-53-4Relevant articles and documents

METHOD FOR PREPARING DIFLUOROACETIC ACID ESTERS

-

Page/Page column 8, (2012/07/31)

A method for preparing difluoroacetic acid esters is described. The method can include reacting difluoroacetyl fluorine with an aliphatic or cycloaliphatic alcohol in the presence of a heterogeneous mineral base.

Preparation of compounds comprising a CHF2 or CHF group

-

Page/Page column 2; 3, (2008/06/13)

Producing compounds (I) with a mono- or difluoromethyl group from compounds (II) with a mono- or difluorohalomethyl group, where halo is bromo, iodo or preferably chloro, comprises reacting (II) with zinc in the presence of an alcohol. An independent claim is also included for an azeotropic mixture of methyl difluoroacetate and methanol.

ALDOL REACTION OF IODODIFLUOROACETATE-Zn AND 2,2-DIFLUOROKETENE SILYL ACETAL

Kitagawa, Osamu,Taguchi, Takeo,Kobayashi, Yoshiro

, p. 1803 - 1806 (2007/10/02)

Generation of the Reformatsky reagent of difluoroacetate from the iodide(2) and the difluoroketene silyl acetal(3), and their aldol reaction are described.High anti-selectivity with chiral aldehyde (5d, 5f) was found in the case of the ketene silyl acetal(3b). 2,2-Difluoro-2-deoxy analogs of D-ribo- and L-galactopyranosides (1a, 1b) were effectively prepared.

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