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1,3-Pentadiene, 1,1,2,3,4,5,5,5-octafluoro-, (Z)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

105311-65-7

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105311-65-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 105311-65-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,3,1 and 1 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 105311-65:
(8*1)+(7*0)+(6*5)+(5*3)+(4*1)+(3*1)+(2*6)+(1*5)=77
77 % 10 = 7
So 105311-65-7 is a valid CAS Registry Number.

105311-65-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1,2,3,4,5,5,5-octafluoropenta-1,3-diene

1.2 Other means of identification

Product number -
Other names 1,3-Pentadiene,1,1,2,3,4,5,5,5-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:105311-65-7 SDS

105311-65-7Downstream Products

105311-65-7Relevant academic research and scientific papers

Kinetic and Thermodynamic Studies of the Thermal Electrocyclic Interconversions of Perfluorinated Dienes and Cyclobutenes

Dolbier, Jr., William R.,Koroniak, Henryk,Burton, Donald J.,Heinze, Pamela L.,Bailey, A.R.,et al.

, p. 219 - 225 (1987)

Detailed kinetic and thermodynamic analyses were carried out for the thermal interconversions of (Z,Z)- and (E,E)-perfluoro-2,4-hexadienes with trans-perfluoro-3,4-dimethylcyclobutene, (E,Z)-perfluoro-2,4-hexadiene with perfluoro-cis-3,4-dimethylcyclobutene, (Z,Z)- and (E,E)-perfluoro-3,5-octadienes with trans-perfluoro-3,4-diethylcyclobutene, and (Z)- and (E)-perfluoro-1,3-pentadiene with perfluoro-3-methylcyclobutene.In each case the (Z,Z)- or (Z)-dienes exhibited substantial kinetic advantage over the (E,E)-or (E)-dienes in their cyclization precesses.

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