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1,1-diphenyl-2,2-ditolylethanediol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

63838-73-3

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63838-73-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 63838-73-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,8,3 and 8 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 63838-73:
(7*6)+(6*3)+(5*8)+(4*3)+(3*8)+(2*7)+(1*3)=153
153 % 10 = 3
So 63838-73-3 is a valid CAS Registry Number.

63838-73-3SDS

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-diphenyl-2,2-ditolylethanediol

1.2 Other means of identification

Product number -
Other names 1,1-diphenyl-2,2-di-p-tolyl-ethane-1,2-diol

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:63838-73-3 SDS

63838-73-3Relevant academic research and scientific papers

Tetraarylethanediols: Surprisingly Low Energy Requirements for Electron Transfer in Solution and in the Gas Phase

Penn, John H.,Lin, Zhe,Deng, Dao-Li

, p. 1001 - 1008 (2007/10/02)

A number of methyl-substituted tetraarylethanediols 1 have been found to undergo facile electron transfer (et) to tris(1,10-phenanthroline)iron(III) complexes (FeIIIL3).The products of this reaction are the corresponding benzophenones when an appropriate base is added to the reaction solution.The electron-transfer rate constants (ket) for the reaction of 1 and FeIIIL3 have been measured as a function of temperature and are higher than anticipated, based on the energetic predictions derived from model arenes.The oxidation potential, derived from the measured ΔGet*, is in good agreement with the solution-phase ΔGeto, which can be calculated from the gas-phase ionization potential.Control experiments demonstrate that the reaction proceeds through a normal outer-sphere electron-transfer reaction.The surprisingly low oxidation potentials can only be explained by through-space phenyl-phenyl interactions.

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