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261503-74-6

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261503-74-6 Usage

Description

8H,8H-Perfluoropentadecane-7,9-dione is a chemical compound characterized by its perfluorinated structure and dione functionality. It is known for its unique properties, such as high thermal stability and chemical inertness, which make it suitable for various applications in different industries.

Uses

Used in Chemical Industry:
8H,8H-Perfluoropentadecane-7,9-dione is used as a precursor for the preparation of transition metal Perfluoroalkyl-derivatized β-diketonato complexes. These complexes are important in various applications, such as catalysts, magnetic materials, and advanced coatings, due to their unique properties and reactivity.
Used in Catalysts:
In the field of catalysis, 8H,8H-Perfluoropentadecane-7,9-dione is used to synthesize transition metal complexes that exhibit enhanced catalytic activity and selectivity. These complexes can be employed in various chemical reactions, such as olefin polymerization, hydrogenation, and oxidation processes, where they can improve the efficiency and performance of the catalysts.
Used in Magnetic Materials:
8H,8H-Perfluoropentadecane-7,9-dione is also utilized in the development of magnetic materials, where the transition metal complexes derived from this compound can exhibit unique magnetic properties. These materials can be used in various applications, such as data storage devices, sensors, and electronic components, where their magnetic properties can be exploited for improved performance.
Used in Advanced Coatings:
The transition metal Perfluoroalkyl-derivatized β-diketonato complexes prepared from 8H,8H-Perfluoropentadecane-7,9-dione can be used in the formulation of advanced coatings with exceptional properties, such as high chemical resistance, low friction, and excellent thermal stability. These coatings can be applied in various industries, including aerospace, automotive, and electronics, to provide protection and enhanced performance for various components and structures.

Check Digit Verification of cas no

The CAS Registry Mumber 261503-74-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,1,5,0 and 3 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 261503-74:
(8*2)+(7*6)+(6*1)+(5*5)+(4*0)+(3*3)+(2*7)+(1*4)=116
116 % 10 = 6
So 261503-74-6 is a valid CAS Registry Number.
InChI:InChI=1/C15H2F26O2/c16-4(17,6(20,21)8(24,25)10(28,29)12(32,33)14(36,37)38)2(42)1-3(43)5(18,19)7(22,23)9(26,27)11(30,31)13(34,35)15(39,40)41/h1H2

261503-74-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1,1,2,2,3,3,4,4,5,5,6,6,10,10,11,11,12,12,13,13,14,14,15,15,15-hexacosafluoropentadecane-7,9-dione

1.2 Other means of identification

Product number -
Other names PC4701

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:261503-74-6 SDS

261503-74-6Downstream Products

261503-74-6Relevant articles and documents

Synthesis and coordination chemistry of perfluoroalkyl-derivatised β-diketonates

Croxtal, Ben,Fawcett, John,Hope, Eric G.

, p. 65 - 73 (2003)

A series of fluorinated β-diketones, RfC(O)CH2C(O)Rf′ (Rf = C6F13, Rf′ = CF3; Rf = Rf′ = C6F13, C7F15), have been prepared in reasonable yields by a two-step synthesis. On reaction with appropriate metal substrates deprotonation and concurrent coordination of the perfluoroalkyl-derivatised β-diketonate ligands affords a range of fluorous metal complexes which have been characterised by elemental analysis, mas spectrometry, IR and NMR spectroscopies. The structures of [Cu(L-L)2(H2O)2] {L-L = CF3C(O)CHC(O)C6F13, C6F13C(O)CHC(O)C6F13}.

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