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Cyclohexene, 1,3,3,4,4,5,5,6,6-nonafluoro-2-iodo- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

14315-34-5

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14315-34-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14315-34-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,3,1 and 5 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 14315-34:
(7*1)+(6*4)+(5*3)+(4*1)+(3*5)+(2*3)+(1*4)=75
75 % 10 = 5
So 14315-34-5 is a valid CAS Registry Number.

14315-34-5SDS

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 1,3,3,4,4,5,5,6,6-nonafluoro-2-iodocyclohexene

1.2 Other means of identification

Product number -
Other names 1-iodononafluorocyclohexene

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:14315-34-5 SDS

14315-34-5Downstream Products

14315-34-5Relevant academic research and scientific papers

A widely varying range of products in reactions of C6F5BrF2, C6F5IF2, and C6F5IF4 with Lewis acids of different strength

Frohn, Hermann-Josef,Bailly, Frank,Welting, Dirk,Bardin, Vadim V.

experimental part, p. 301 - 307 (2009/12/04)

The relative fluoride donor ability: C6F5BrF2 > C6F5IF2 > C6F5IF4 was outlined from reactions with Lewis acids of graduated strength in different solvents.

The first hydrogen containing (polyfluorocycloalken-1-yl)xenon(II) salts

Frohr,Bardin

, p. 562 - 564 (2007/10/03)

(2-H-Hexafluoro-1,4-cyclohexadien-1-yl)xenon(II) and (2-H-octafluorocyclohexen-1-yl)xenon(II) hexafluoroarsenates and tetrafluoroborates were obtained together with their perfluorinated analogues on reacting the corresponding (2,3,4,5-tetrarluorophenyl)xenon(II) salts with XeF2 in anhydrous HF (aHF). The fluorinated (cyclohexen-1-yl)xenon(II) cations react with bromide and iodide anions in MeCN and aHF under alkenylation of the halide anions.

FLUORINATION OF POLYFLUOROAROMATIC COMPOUNDS WITH VANADIUM PENTAFLUORIDE

Bardin, V. V.,Avramenko, A. A.,Furin, G. G.,Yakobson, G. G.,Krasilnikov, V. A.,et al.

, p. 37 - 46 (2007/10/02)

Fluorination of polyfluoro-derivatives of benzene and diphenyl with vanadium pentafluoride at -25 to -10 deg C afforded fluorinated cyclohexadienes and cyclohexenes.Octafluoronaphthalene was converted under these conditions to perfluoro-1,4-dihydronaphthalene, perfluorotetralin, perfluoro-1,4,5,8-tetrahydronaphthalene and perfluoro-1,2,3,4,5,8-hexahydronaphthalene.

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