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[13C]hydrogen cyanide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

20722-83-2

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20722-83-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20722-83-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,7,2 and 2 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 20722-83:
(7*2)+(6*0)+(5*7)+(4*2)+(3*2)+(2*8)+(1*3)=82
82 % 10 = 2
So 20722-83-2 is a valid CAS Registry Number.

20722-83-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name [13C]hydrogen cyanide

1.2 Other means of identification

Product number -
Other names (13)C-hydrocyanic acid

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:20722-83-2 SDS

20722-83-2Relevant academic research and scientific papers

Mass Spectrometric Investigation of Nitrogen Compounds, XXXV. Phenyl-substituted 2-Azaallenium Ions in the Gas Phase

Wuerthwein, Ernst-Ullrich,Halim, Herman,Schwarz, Helmut,Nibbering, Nico M. M.

, p. 2626 - 2634 (2007/10/02)

The gas phase chemistry of metastable phenyl-substituted 2-azaallenium ions (2a, b, c) is characterized by intramolecular electrophilic substitution reactions; these processes are energetically favoured in comparison with various phenyl and hydrogen migrations, in spite of the fact that the latter may give rise to the formation of more stable intermediates (nitrilium ions).As a direct consequence of the electrophilic substitution, 2a, c decompose via loss of HCN, whereas from 2b PhCN is eliminated unimolecularly.The combination of experimental investigations, employing - and -labelled precursors, and MNDO calculations allows to give a detailed description of the chemistry of isolated 2a, b, c cations.

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