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40723-64-6

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40723-64-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 40723-64-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,7,2 and 3 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 40723-64:
(7*4)+(6*0)+(5*7)+(4*2)+(3*3)+(2*6)+(1*4)=96
96 % 10 = 6
So 40723-64-6 is a valid CAS Registry Number.

40723-64-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1,2,2,3,3,4,4-octafluoropentane

1.2 Other means of identification

Product number -
Other names Pentane,1,1,2,2,3,3,4,4-octafluoro

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:40723-64-6 SDS

40723-64-6Downstream Products

40723-64-6Relevant articles and documents

SYNTHESIS OF FLUORINATED OLEFINS FROM FLUORINATED ALCOHOLS

-

Page/Page column 6-7, (2011/08/08)

Disclosed is a process for producing a hydrofluoroalkene, RfCF=CH2 comprising contacting a hydrofluoroalkanol of structure RfCF2CH2OH, with a lewis acid to produce a mixture, diluting said mixture with a solvent to produce a solvent mixture, contacting the solvent mixture with a reactive metal, heating the solvent mixture and reactive metal for a sufficient amount of time to produce a hydrofluoroalkene, and condensing and collecting the volatile products comprising the hydrofluoroalkene, wherein Rf is F, or a fluorine-substituted alkyl group.

Reductive dehalogenation of polyhalofluorocarbons with tributyltin hydride

Puy, Michael Van Der,Belter, Randolph K.,Borowski, Ralph J.,Ellis, Lois A. S.,Persichini, Phillip J.,et al.

, p. 59 - 64 (2007/10/02)

The reduction of polyhalofluorocarbons, including ClCF2CFClCF2Cl, (ClCF2CFCl)2, ICH2(CF2)3CH2I and vicinal dichloroperfluorocycloalkanes, with tributyltin hydride gave the corresponding hydrofluorocarbons in good to excellent yield.The results are compared with similar reductions with other reducing agents, and to tin hydride reductions of non-fluorinated analogs. - Keywords: Reductive dehalogenation; Polyfluorocarbons; Tributyltin hydride; NMR spectroscopy; Hydrofluorocarbons

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