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14039-18-0

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14039-18-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14039-18-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,0,3 and 9 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 14039-18:
(7*1)+(6*4)+(5*0)+(4*3)+(3*9)+(2*1)+(1*8)=80
80 % 10 = 0
So 14039-18-0 is a valid CAS Registry Number.

14039-18-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name p-Methoxyphenyl-diphenylmethyliumion

1.2 Other means of identification

Product number -
Other names <4-Methoxy-phenyl>-diphenyl-methyl-Kation

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:14039-18-0 SDS

14039-18-0Relevant articles and documents

1H and 13C NMR detection of the carbocations or zwitterions from Rhodamine B base, a fluoran-based black color former, trityl benzoate, and methoxy-substituted trityl chlorides in the presence of alkali metal or alkaline earth metal

Hojo, Masashi,Ueda, Tadaharu,Yamasaki, Masanori,Inoue, Akihiko,Tokita, Sumio,Yanagita, Mitsuhiro

, p. 1569 - 1576 (2007/10/03)

The cleavage of C-O bonds in two fluoran-based dyes by the addition of alkali metal (M+ = Li+, Na+) and alkaline earth metal (M2+ = Mg2+, Ba2+) perchlorates in acetonitrile solution was exa

The Effect of Both ?-Donor Substituents and Acid Media on the Formation of Trityl Cations, Studied by Relaxation Methods and NMR-Spectroscopy

Blumenstock, H.,Dickert, F.,Fackler, H.,Hammerschmidt, A.

, p. 157 - 170 (2007/10/02)

Trityl trifluoroacetates were taken to study why ion formation from ionogens is favoured by acid media.From relaxation measurements, NMR-spectroscopy and conductivity studies it was found that this effect is due to anion solvation by acid, namely a specific solvation of the free anions and a statistical solvation of the anions bound in the ionogen.This leads to a drastically reduced ion recombination rate constant even at low concentrations of acid and an increased dissociation rate constant at rather high concentrations of acid. -.Keywords: Kinetics/ Ion solvation/ Carbenium ions/ NMR-spectroscopy

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