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1,1,1,5,5,6,6,7,7,7-Decafluoro-2,4-heptanedione is a perfluorinated chemical compound characterized by the molecular formula C7F10O. It features ten fluorine atoms and two carbonyl groups, which confer high stability and resistance to chemical reactions. 1,1,1,5,5,6,6,7,7,7-DECAFLUORO-2,4-HEPTANEDIONE is recognized for its unique chemical properties and is utilized as a key building block in the synthesis of various fluorinated organic compounds and materials.

20583-66-8

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20583-66-8 Usage

Uses

Used in Chemical Synthesis:
1,1,1,5,5,6,6,7,7,7-Decafluoro-2,4-heptanedione is used as a building block for the synthesis of fluorinated organic compounds, leveraging its stability and reactivity to create a range of specialized products.
Used in Material Production:
1,1,1,5,5,6,6,7,7,7-DECAFLUORO-2,4-HEPTANEDIONE serves as a precursor in the production of fluorinated materials, which are known for their exceptional properties such as non-stick surfaces, heat resistance, and chemical inertness.
Used in Electronic Materials Industry:
1,1,1,5,5,6,6,7,7,7-Decafluoro-2,4-heptanedione is used as a component in the development of electronic materials, where its stability and fluorine content contribute to the performance of these materials in various electronic applications.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 1,1,1,5,5,6,6,7,7,7-DECAFLUORO-2,4-HEPTANEDIONE is utilized as an intermediate in the synthesis of fluorinated drugs, taking advantage of its chemical properties to enhance the efficacy and stability of pharmaceutical products.
Used in Specialty Chemicals Industry:
1,1,1,5,5,6,6,7,7,7-Decafluoro-2,4-heptanedione is employed in the formulation of specialty chemicals, where its unique characteristics are harnessed to create high-performance chemical products for specific applications.
It is crucial to handle 1,1,1,5,5,6,6,7,7,7-Decafluoro-2,4-heptanedione with care due to its potential environmental and health risks, including persistence and bioaccumulation concerns. Proper management and disposal methods are essential to mitigate any adverse effects on the environment and human health.

Check Digit Verification of cas no

The CAS Registry Mumber 20583-66-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,5,8 and 3 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 20583-66:
(7*2)+(6*0)+(5*5)+(4*8)+(3*3)+(2*6)+(1*6)=98
98 % 10 = 8
So 20583-66-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H2F10O2/c8-4(9,6(13,14)7(15,16)17)2(18)1-3(19)5(10,11)12/h1H2

20583-66-8 Well-known Company Product Price

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  • Alfa Aesar

  • (L09724)  1,1,1,5,5,6,6,7,7,7-Decafluoro-2,4-heptanedione, 97%   

  • 20583-66-8

  • 1g

  • 227.0CNY

  • Detail
  • Alfa Aesar

  • (L09724)  1,1,1,5,5,6,6,7,7,7-Decafluoro-2,4-heptanedione, 97%   

  • 20583-66-8

  • 5g

  • 865.0CNY

  • Detail
  • Alfa Aesar

  • (L09724)  1,1,1,5,5,6,6,7,7,7-Decafluoro-2,4-heptanedione, 97%   

  • 20583-66-8

  • 25g

  • 3320.0CNY

  • Detail

20583-66-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1,1,5,5,6,6,7,7,7-decafluoroheptane-2,4-dione

1.2 Other means of identification

Product number -
Other names 3H,3H-Perfluoro-2,4-heptanedione

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:20583-66-8 SDS

20583-66-8Downstream Products

20583-66-8Relevant academic research and scientific papers

Reaction of 3H-perfluoroalk-2-enes with ammonia

Petrova,Kurykin

, p. 155 - 156 (2001)

3H-Perfluoroalk-2-enes react with aqueous ammonia to form polyfluorinated iminoenamines, from which hexafluoroacetylacetone and its analogs were synthesized.

New efficient synthetic routes to trifluoromethyl substituted pyrazoles and corresponding β-diketones

Grünebaum, Mariano,Buchheit, Annika,Günther, Christina,Wiemh?fer, Hans-D.

supporting information, p. 1555 - 1559 (2018/03/29)

An improved and more efficient synthesis procedure for trifluoromethyl substituted pyrazoles, namely 3,5-bis(trifluoromethyl)-1H-pyrazole (1a), 5-(pentafluoroethyl)-3-(trifluoromethyl)-1H-pyrazole (1b), 5-(heptafluoropropyl)-3-(trifluoromethyl)-1H-pyrazol

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