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Naphthalene, 1,1,2,2,3,3,4,4-octafluoro-1,2,3,4-tetrahydro- is a synthetic chemical compound with the molecular formula C10H4F8. It is a fluorinated derivative of naphthalene, a polycyclic aromatic hydrocarbon. Naphthalene, 1,1,2,2,3,3,4,4-octafluoro-1,2,3,4-tetrahydro- is characterized by the presence of eight fluorine atoms and four hydrogen atoms, with the fluorine atoms replacing hydrogen atoms in the naphthalene structure. Due to its unique properties, such as high thermal stability and chemical resistance, it has potential applications in various fields, including materials science, pharmaceuticals, and as a precursor in the synthesis of other fluorinated compounds. However, it is important to note that the compound may have potential health and environmental risks, and further research is needed to fully understand its impact.

3262-14-4

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3262-14-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3262-14-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,6 and 2 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3262-14:
(6*3)+(5*2)+(4*6)+(3*2)+(2*1)+(1*4)=64
64 % 10 = 4
So 3262-14-4 is a valid CAS Registry Number.

3262-14-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1,2,2,3,3,4,4-octafluoro-1,2,3,4-tetrahydronaphthalene

1.2 Other means of identification

Product number -
Other names Benzo-perfluorcyclohexan

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:3262-14-4 SDS

3262-14-4Relevant academic research and scientific papers

THERMOLYTIC TRANSFORMATION OF POLYFLUORINATED ORGANIC COMPOUNDS. XXVIII. PRODUCTION OF POLYFLUOROINDANES AND SOME OF THEIR CHARACTERISTICS

Platonov, V. E.,Malyuta, N. G.,Yakobson, G. G.

, p. 345 - 353 (2007/10/02)

The copyrolysis (620 deg C) of phenol and ortho- and para-halogenophenols with perfluoroethylene in a flow-type system was investigated. 1,1,2,2,3,3-hexafluoroindane was mostly obtained from phenol, anisole, and o-bromophenol; o-chlorophenol gives the same compounds as the main product together with 1,1,2,2,3,3-hexafluoro-4-chloroindane; in the case of o-fluorophenol the main reaction products are 1,1,2,2,3,3-hexafluoroindane and 1,1,2,2,3,3,4- and 1,1,2,2,3,3,5-heptafluoroindanes.With perfluoroethylene para-halogenophenols form 1,1,2,2,3,3-hexafluoro-5-halogenoindanes.The paths to the formation of the polyfluoroindanes are discussed.When heated with nitric acid, 1,1,2,2,3,3-hexafluoroindane gives mainly 4-nitro-1,1,2,2,3,3-hexafluoroindane, from which the corresponding amino derivative is obtained by reduction.

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