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Benzoyl chloride, 4,4'-[(1,2,3,3,4,4-hexafluoro-1,2-cyclobutanediyl)bis(oxy)]bis- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

129844-91-3

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129844-91-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 129844-91-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,8,4 and 4 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 129844-91:
(8*1)+(7*2)+(6*9)+(5*8)+(4*4)+(3*4)+(2*9)+(1*1)=163
163 % 10 = 3
So 129844-91-3 is a valid CAS Registry Number.

129844-91-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2-Bis (4-Chloroformylphenoxy)Hexafluorocyclobutane

1.2 Other means of identification

Product number -
Other names 1,2-bis(4-chloroformylphenoxy)-hexafluorocyclobutane

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:129844-91-3 SDS

129844-91-3Upstream product

129844-91-3Relevant academic research and scientific papers

Reactive compounds containing perfluorocyclobutane rings

-

, (2008/06/13)

Novel compounds have at least one perfluorocyclobutane ring and at least two functional groups suitable for forming condensation polymers. Preferably the compounds have a structures represented by Formula II: STR1 wherein R and R' independently represent optionally inertly substituted groups; X and X' represent any molecular structures which link R and R' with the perfluorocyclobutane ring; n and n' are the number of G and G' groups, respectively; and G and G' independently represent any reactive functional groups or any groups convertible into reactive functional groups. The compound are preferably prepared by a process of thermally dimerizing trifluorovinyl compound to form a compounds of Formula I wherein G represents G or G' in Formula II; X represents X or X' of Formual II; and n represents n or n' of Formula II, to form a compound having a perfluorocyclobutane group.

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