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Perfluoroperhydrofluoranthene is a synthetic, fully fluorinated polycyclic aromatic hydrocarbon (PAH) with the chemical formula C18F18. It is a derivative of perhydrofluoranthene, where all hydrogen atoms are replaced by fluorine atoms. perfluoroperhydrofluoranthene is characterized by its high thermal stability, chemical inertness, and unique electronic properties. Due to its resistance to degradation and low reactivity, perfluoroperhydrofluoranthene has potential applications in various fields, such as materials science, electronics, and as a reference compound in analytical chemistry. However, it is important to note that, like other perfluorinated compounds, it may have environmental and health concerns due to its persistence and potential bioaccumulation.

662-28-2

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662-28-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 662-28-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,6 and 2 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 662-28:
(5*6)+(4*6)+(3*2)+(2*2)+(1*8)=72
72 % 10 = 2
So 662-28-2 is a valid CAS Registry Number.
InChI:InChI=1/C16F26/c17-1-2(18)4(20)5(21,10(29,30)16(41,42)15(39,40)9(4,27)28)3(1,19)8(25,26)14(37,38)12(33,34)6(1,22)11(31,32)13(35,36)7(2,23)24

662-28-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1,2,2,3,3,3a,4,4,5,5,6,6,6a,6b,7,7,8,8,9,9,10,10,10a,10b,10c-hexacosafluorofluoranthene

1.2 Other means of identification

Product number -
Other names hexacosafluoro-hexadecahydro-fluoranthene

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:662-28-2 SDS

662-28-2Upstream product

662-28-2Relevant academic research and scientific papers

Polycyclic Fluoro-aromatic Compounds. Part 9. Preparation and Some Reactions of Decafluorofluoranthene

Burdon, James,Gill, Harpal S.,Parsons, Ian W.,Tatlow, John Colin

, p. 1726 - 1730 (2007/10/02)

Fluorinations of fluoranthene with cobalt trifluoride and potassium tetrafluorocobaltate give perfluoroperhydrofluoranthene and perfluorotetradecahydrofluoranthene, respectively.Defluorination of either of these over iron(III) oxide gives decafluorofluoranthene, which is attacked by nucleophiles (OMe-, H-, NH2NH2) at position 1,and then at 6, 3, and 4.Oxidation of decafluorofluoranthene with nitric acid gives octafluorofluoranthene-2,3-quinone and then heptafluoro-9-oxofluorene-1-carboxylic acid.

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