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355-68-0

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355-68-0 Usage

Purification Methods

Extract it repeatedly with MeOH, then pass it through a column of silica gel (previously activated by heating at 250o). [Haszeldine & Smith J Chem Soc 2691 1950, IR: Thompson & Temple J Chem Soc 1432 1948, Beilstein 5 III 37, 5 IV 48.]

Check Digit Verification of cas no

The CAS Registry Mumber 355-68-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,5 and 5 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 355-68:
(5*3)+(4*5)+(3*5)+(2*6)+(1*8)=70
70 % 10 = 0
So 355-68-0 is a valid CAS Registry Number.
InChI:InChI=1S/C6F12/c7-1(8)2(9,10)4(13,14)6(17,18)5(15,16)3(1,11)12

355-68-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1,2,2,3,3,4,4,5,5,6,6-dodecafluorocyclohexane

1.2 Other means of identification

Product number -
Other names Dodecafluorocyclohexane

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:355-68-0 SDS

355-68-0Relevant articles and documents

-

Christoffers,Lingafelter,Cady

, p. 2502 (1947)

-

PROCESS FOR PREPARING DECAFLUOROCYCLOHEXENE

-

Page/Page column 3, (2010/06/11)

Disclosed herein is a process of preparing decafluorocyclohexene using hexafluorobenzene as a raw material. The hexafluorobenzene reacts with an activated fluorinating agent at 60-200° C. in an inert gas atmosphere. The activated fluorinating agent is prepared by mixing 1-50 wt % of cobalt difluoride with 50-99 wt % of other metal fluoride selected from calcium fluoride, magnesium fluoride, aluminum fluoride, sodium fluoride and potassium fluoride. The mixture reacts with fluorine gas at 200-400° C.

Electrochemical fluorination of unsaturated sulfides and sulfones

Grigor'eva,Shainyan,Kaurova,Gracheva,Lesnevskaya,Barabanov

, p. 1095 - 1100 (2007/10/03)

Electrochemical fluorination of some unsaturated sulfides and sulfones and their reactions with anhydrous HF were studied.

Skeletal Rearrangements during the Fluorination of C6-Hydrocarbons over Cobalt(III) Trifluoride

Burdon, James,Creasey, Jeremy C.,Proctor, Lee D.,Plevey, Raymond G.,Yeoman, J.R. Neil

, p. 445 - 447 (2007/10/02)

Perfluorination of hexane, 2-methylpentane, 3-methylpentane, 2,2-dimethylbutane, 2,3-dimethylbutane, methylcyclopentane and cyclohexane over cobalt(III) trifluoride gave, in each case except perhaps cyclohexane, a mixture of linear, branched and cyclic C6-fluorocarbons: the degree of skeletal rearrangement (excluding cyclohexane) varied from ca. 7percent (methylcyclopentane) to 96percent (2,2-dimethylbutane).A carbocation mechanism, which does not proceed to equilibrium, is suggested.

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