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Methylium, fluorophenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

56683-64-8

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56683-64-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56683-64-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,6,8 and 3 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 56683-64:
(7*5)+(6*6)+(5*6)+(4*8)+(3*3)+(2*6)+(1*4)=158
158 % 10 = 8
So 56683-64-8 is a valid CAS Registry Number.

56683-64-8SDS

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 fluoro-phenyl-methylium

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:56683-64-8 SDS

56683-64-8Downstream Products

56683-64-8Relevant academic research and scientific papers

Mass-Spectrometric Study on Ion-Molecule Reactions of CF3+ with Monosubstituted Benzenes Carrying a Carbonyl Group at Near-Thermal Energies

Tsuji, Masaharu,Aizawa, Masato,Nishimura, Yukio

, p. 1055 - 1063 (1996)

The gas-phase ion-molecule reactions of CF3+ with five monosubstituted benzenes carrying a carbonyl group (PhCOX: X=H, CH3, C2H5, OCH3, OC2H5) have been studied at near-thermal energies using an ion-beam apparatus. The major product channel for PhCHO, PhCOCH3, and PhCOOCH3 is electrophilic addition to the O-atom leading to initial adduct ions, which are 80.3 - 95.0% of the total product ions. Although no initial adduct ions are observed for PhCOC2H5 and PhCOOC2H5, major product ions are formed by electrophilic addition to the O-atom followed by dissociation and molecular eliminations. The reaction mechanism is discussed based on product ion distributions and semi-empirical calculations of the energies of intermediates and products. The results obtained are compared with reported-ion-cyclotron-resonance data for aliphatic carbonyl compounds.

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