1620487-87-7 Usage
Description
(E)-1,2-Bis(1-naphthyl)-1,2-bis(1,1,3,3,5,5,7,7-octaethyl-1,2,3,5,6,7-hexahydro-s-indacen-4-yl)disilene is a complex organosilicon compound characterized by its unique molecular structure. It features two naphthyl groups and two s-indacen-4-yl groups connected by a silicon-silicon double bond, which contributes to its potential applications in various fields.
Uses
Used in Materials Science:
(E)-1,2-Bis(1-naphthyl)-1,2-bis(1,1,3,3,5,5,7,7-octaethyl-1,2,3,5,6,7-hexahydro-s-indacen-4-yl)disilene is used as a precursor for developing new materials with specific functionalities due to its unique structure and organosilicon nature.
Used in Organic Synthesis:
(E)-1,2-Bis(1-naphthyl)-1,2-bis(1,1,3,3,5,5,7,7-octaethyl-1,2,3,5,6,7-hexahydro-s-indacen-4-yl)disilene is used as a reactive intermediate in organic synthesis, taking advantage of its silicon-silicon double bond to facilitate various chemical reactions and the formation of new compounds.
Used in Electronic and Optical Property Research:
(E)-1,2-Bis(1-naphthyl)-1,2-bis(1,1,3,3,5,5,7,7-octaethyl-1,2,3,5,6,7-hexahydro-s-indacen-4-yl)disilene is used as a subject of study for its electronic and optical properties, which could lead to advancements in the development of electronic devices and optical materials.
Used in Catalysis:
It is also utilized in the field of catalysis, where its organosilicon framework may offer novel catalytic properties and contribute to the development of more efficient catalytic processes.
Check Digit Verification of cas no
The CAS Registry Mumber 1620487-87-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,2,0,4,8 and 7 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1620487-87:
(9*1)+(8*6)+(7*2)+(6*0)+(5*4)+(4*8)+(3*7)+(2*8)+(1*7)=167
167 % 10 = 7
So 1620487-87-7 is a valid CAS Registry Number.
1620487-87-7Relevant articles and documents
Highly coplanar (E)-1,2-Di(1-naphthyl)disilene involving a distinct CH-π interaction with the perpendicularly oriented protecting eind group
Kobayashi, Megumi,Hayakawa, Naoki,Nakabayashi, Koichi,Matsuo, Tsukasa,Hashizume, Daisuke,Fueno, Hiroyuki,Tanaka, Kazuyoshi,Tamao, Kohei
, p. 432 - 434 (2014)
An air-stable emissive di(1-naphthyl)disilene protected by the bulky Eind groups (Eind: 1,1,3,3,5,5,7,7-octaethyl-s-hydrindacen-4-yl) has been obtained by reducing the corresponding dibromosilane (Eind)(1-Naph)SiBr2 with lithium naphthalenide. The X-ray crystallography shows a highly coplanar (E)-1,2-di-(1-naphthyl)disilene skeleton, favorable for the efficient π-conjugation involving the Si=Si unit, together with a distinct CHπ interaction between the peri-H atom of 1-naphthyl groups and the aromatic ring of the perpendicularly oriented Eind groups.
