18064-78-3 Usage
General Description
Diselenide, bis(pentafluorophenyl) is a chemical compound with the molecular formula (C6F5)2Se2. It is a selenium-based compound that is used in a variety of chemical reactions and processes. The compound is characterized by its two pentafluorophenyl groups attached to the selenium atoms. It is known for its reactivity and ability to participate in various organic synthesis reactions. Diselenide, bis(pentafluorophenyl) has been studied for its potential applications in materials science, catalysis, and medicinal chemistry. It is important to handle this compound with caution as it may pose health hazards and is toxic if ingested or inhaled.
Check Digit Verification of cas no
The CAS Registry Mumber 18064-78-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,0,6 and 4 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 18064-78:
(7*1)+(6*8)+(5*0)+(4*6)+(3*4)+(2*7)+(1*8)=113
113 % 10 = 3
So 18064-78-3 is a valid CAS Registry Number.
18064-78-3Relevant articles and documents
Diselenide-Mediated Catalytic Functionalization of Hydrophosphoryl Compounds
Handoko,Benslimane, Zacharia,Arora, Paramjit S.
, p. 5811 - 5816 (2020/07/27)
We report a diaryldiselenide catalyst for cross-dehydrogenative nucleophilic functionalization of hydrophosphoryl compounds. The proposed organocatalytic cycle closely resembles the mechanism of the Atherton-Todd reaction, with the catalyst serving as a recyclable analogue of the halogenating agent employed in the named reaction. Phosphorus and selenium NMR studies reveal the existence of a P-Se bond intermediate, and structural analyses indicate a stereospecific reaction.
Reactions of Monocyclopentadienyl Complexes of Molybdenum and Tungsten with Derivatives of Phenols and Pentafluorobenzeneselenol
Davidson, Jack L.,Holz, Birgit,Leverd, Pascal C.,Lindsell, W. Edward,Simpson, Nigel J.
, p. 3527 - 3532 (2007/10/02)
Reactions of (cp = η5-C5H5) with thallium salts Tl(OR) (R = aryl) in tetrahydrofuran did not produce simple substitution products but afforded reduced species 2, oxidised species or the thalliu
