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1119-20-6

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1119-20-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1119-20-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,1 and 9 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1119-20:
(6*1)+(5*1)+(4*1)+(3*9)+(2*2)+(1*0)=46
46 % 10 = 6
So 1119-20-6 is a valid CAS Registry Number.
InChI:InChI=1/2C2H3.Hg/c2*1-2;/h2*1H,2H2;/rC4H6Hg/c1-3-5-4-2/h3-4H,1-2H2

1119-20-6SDS

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 bis(ethenyl)mercury

1.2 Other means of identification

Product number -
Other names diethynylmercury

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:1119-20-6 SDS

1119-20-6Related news

Syntheses of functionally substituted DIVINYLMERCURY (cas 1119-20-6) compounds09/09/2019

Reductive disproportionation of vinylmercuric chlorides by alkaline sodium stannite produces divinylmercurials in high yields. The reaction conditions are optimized to obtain functionally substituted divinylmercurials in pure form, free from undesirable side products.detailed

1119-20-6Relevant articles and documents

Vinylmercury Hydrides: Synthesis and Spectroscopic Characterization

Guillemin, Jean-Claude,Bellec, Nathalie,Szetsi, Sandor Kis,Nyulaszi, Laszlo,Veszpremi, Tamas

, p. 6586 - 6591 (2008/10/09)

The first vinylmercury hydrides, and among them the parent compound, have been prepared by a chemoselective reduction of the corresponding vinylmercury chlorides with tributylstannane in the presence of a radical inhibitor. These hydrides have been characterized on the basis of their spectral data (1H, 13C, and 199Hg NMR spectroscopy and mass spectrometry). The photoelectron spectra of the ethenylmercury hydride displays bands at 9.79,10.13, 11.41, and 13.20 eV. On the basis of photoelectron spectra and ab initio quantum chemical calculations some (d-p)π interaction between the vinyl π-system and the mercury d-orbitals could be concluded. Vinylmercury hydrides have been condensed and then revaporized in vacuum at low temperature, but they exhibit a very low stability at room temperature even diluted in toluene (τ1/2 ≈ l min); elemental mercury and the corresponding divinylmercury were formed under these conditions.

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