3294-57-3 Usage
Description
PHENYL(TRICHLOROMETHYL)MERCURY is a synthetic organic chemical compound that consists of a phenyl group, a trichloromethyl group, and a mercury atom. It is often utilized as a reagent in various organic chemistry reactions. However, it is also recognized for its toxic properties, as mercury compounds are widely known for their detrimental effects on human health and the environment.
Uses
Used in Organic Chemistry:
PHENYL(TRICHLOROMETHYL)MERCURY is used as a reagent in organic chemistry for facilitating specific chemical reactions. Its unique structure allows it to participate in various synthesis processes, contributing to the formation of desired products.
Used in Research and Development:
Due to its reactivity and the potential for creating new compounds, PHENYL(TRICHLOROMETHYL)MERCURY is also used in research and development settings. Scientists and chemists may explore its properties and reactions to discover new applications or to improve existing chemical processes.
Check Digit Verification of cas no
The CAS Registry Mumber 3294-57-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,9 and 4 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3294-57:
(6*3)+(5*2)+(4*9)+(3*4)+(2*5)+(1*7)=93
93 % 10 = 3
So 3294-57-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H5.CCl3.Hg/c1-2-4-6-5-3-1;2-1(3)4;/h1-5H;;/rC7H5Cl3Hg/c8-7(9,10)11-6-4-2-1-3-5-6/h1-5H
3294-57-3Relevant articles and documents
Nucleophilic cleavage of the Si-C bond in organotrifluorosilanes and diorganodifluorosilanes
Voronkov, M. G.,Chermov, N. F.,Perlova, E. M.
, p. 225 - 230 (2007/10/02)
The Si-C bond in aryltrifluorosilanes, 4-XC6H4SiF3 (X = H, CH3, Cl, Br or NO2), is readily cleaved by mercury(II) salts HgY2 (Y = Cl, Br, I, CN or OCOCH3) or HgO to form organomercurials of the type 4-XC6H4HgY or (4-XC6H4)2Hg, respectively.Electron-donating substituent X facilitate the reaction, whereas electron-withdrawing substituents make it more difficult.Mercury(II) salts and mercury(II) oxide also cleave the Si-C bond in chloromethyltrifluorosilanes, F3Si(CH3-nCln) (n = 1-3) to produce the corresponding organic mercurials containing an Hg(CH3-nCln) group.The substitution of the fluorine atom in organotrifluorosilanes by an alkyl group hinders the bond cleavage between the silicon atom and the electronegative organic substituent.The reactions studied are believed to follow a nucleophilic mechanism involving asynchronous formation of a four-centered transition state with a pentacoordinate silicon atom.
