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N,N-Diethyl-2,3,3,3-tetrafluoropropionamide is a versatile chemical compound characterized by its colorless liquid form, faint sweet odor, and high solubility in organic solvents. It serves as a crucial reagent in organic synthesis and a precursor for the development of pharmaceuticals and agrochemicals, making it a valuable component in the chemical industry.

392-63-2

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392-63-2 Usage

Uses

Used in Organic Synthesis:
N,N-Diethyl-2,3,3,3-tetrafluoropropionamide is used as a reagent in organic synthesis for its ability to facilitate various chemical reactions, contributing to the formation of complex organic compounds.
Used in Pharmaceutical and Agrochemical Production:
In the pharmaceutical industry, N,N-Diethyl-2,3,3,3-tetrafluoropropionamide is used as a precursor in the synthesis of drugs, playing a pivotal role in the development of new medications. Similarly, in agrochemicals, it serves as a starting material for the creation of compounds that protect crops and enhance agricultural productivity.
Used as a Solvent in Chemical Processes:
N,N-Diethyl-2,3,3,3-tetrafluoropropionamide is utilized as a solvent in a range of chemical processes due to its compatibility with organic solvents, which allows for efficient reactions and separations.
Used as a Reaction Intermediate:
N,N-DIETHYL-2,3,3,3-TETRAFLUOROPROPIONAMIDE is also employed as a reaction intermediate in the synthesis of various organic compounds, indicating its multi-step involvement in the creation of complex molecules.
Used in Specialty Chemicals Production:
N,N-Diethyl-2,3,3,3-tetrafluoropropionamide functions as a building block in the production of specialty chemicals, which are often used in niche applications requiring specific chemical properties.
Used in Material Development:
Its applications extend to the development of new materials, where its unique properties can be leveraged to create innovative products with enhanced performance characteristics.
Used in Research and Development of Novel Chemical Processes:
In the realm of research and development, N,N-Diethyl-2,3,3,3-tetrafluoropropionamide is instrumental in exploring and establishing novel chemical processes, potentially leading to breakthroughs in various scientific and industrial fields.

Check Digit Verification of cas no

The CAS Registry Mumber 392-63-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,9 and 2 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 392-63:
(5*3)+(4*9)+(3*2)+(2*6)+(1*3)=72
72 % 10 = 2
So 392-63-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H11F4NO/c1-3-12(4-2)6(13)5(8)7(9,10)11/h5H,3-4H2,1-2H3

392-63-2 Well-known Company Product Price

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  • Alfa Aesar

  • (L16739)  N,N-Diethyl-2,3,3,3-tetrafluoropropionamide, 95%   

  • 392-63-2

  • 25g

  • 647.0CNY

  • Detail
  • Alfa Aesar

  • (L16739)  N,N-Diethyl-2,3,3,3-tetrafluoropropionamide, 95%   

  • 392-63-2

  • 100g

  • 1617.0CNY

  • Detail

392-63-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N-Diethyl-2,3,3,3-tetrafluoropropanamide

1.2 Other means of identification

Product number -
Other names N,N-diethyl-2,3,3,3-tetrafluoropropanamide

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:392-63-2 SDS

392-63-2Relevant academic research and scientific papers

Reactions of 1,1,2,2-tetrafluoroethyl-N,N-dimethylamine with linear and cyclic 1,3-diketones

Grieco, Liane M.,Halliday, Gary A.,Junk, Christopher P.,Lustig, Steven R.,Marshall, William J.,Petrov, Viacheslav A.

experimental part, p. 1198 - 1206 (2011/12/01)

Ketones are known to be unreactive toward α-fluoroamines such as Ishikawa's Reagent or 1,1,2,2-tetrafluoroethyl-N,N-dimethylamine (TFEDMA). On the other hand, 1,3-diketones were found to undergo fluorination with TFEDMA. In the case of linear 1,3-diketone

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