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96759-86-3

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96759-86-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 96759-86-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,7,5 and 9 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 96759-86:
(7*9)+(6*6)+(5*7)+(4*5)+(3*9)+(2*8)+(1*6)=203
203 % 10 = 3
So 96759-86-3 is a valid CAS Registry Number.

96759-86-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1,2,2,3,3,4,4,5,5,6-undecafluoro-6-(trifluoromethyl)cyclohexane

1.2 Other means of identification

Product number -
Other names -

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:96759-86-3 SDS

96759-86-3Relevant articles and documents

Electron Affinities from Electron-Transfer Equilibria : A(-) + B = A + B(-)

Grimsrud, Eric P.,Caldwell, Gary,Chowdhury, Swapan,Kebarle, Paul

, p. 4627 - 4634 (2007/10/02)

Determination of the equilibrium constants K1 for gas-phase electron-transfer equilibria with a pulsed electron beam high ion source pressure mass spectrometer led to the electron affinities of 34 compounds with EA's between 0.5 and 3eV.The compounds are mostly substituted nitrobenzenes, substituted quinones, and conjugated molecules containing oxygen atoms.The EA of smaller molecules like SO2, NO2, CS2, and CH3NO2 also were determined.The method is very well suited for rapid, accurate, routine determinations of electron affinities.A comparison with EA's determined with other gas-phase methods and EA's evaluated from polarographic half-wave reduction potentials and charge-transfer spectra in solution is made.The rate constants for a number of exothermic electron-transfer reactions were determined.Most of these proceed at near collision rates.Electron-transfer reactions involving perfluorinated compounds like perfluoromethylcyclohexane, perfluorocyclohexane, and sulfurhexafluoride do not follow this behavior.While the perfluoro compounds have high thermal electron capture cross sections, they do not accept electrons from A(-) of compounds A with lower electron affinity.The perfluoro anions do transfer electrons to compounds A with higher electron affinity, and the rate constants increase with EA(A) - EA(perfluoro compound).

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