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81795-78-0

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81795-78-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81795-78-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,7,9 and 5 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 81795-78:
(7*8)+(6*1)+(5*7)+(4*9)+(3*5)+(2*7)+(1*8)=170
170 % 10 = 0
So 81795-78-0 is a valid CAS Registry Number.

81795-78-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4-dimethoxy-2,5-bis(2-phenylethenyl)benzene

1.2 Other means of identification

Product number -
Other names trans-2,5-dimethoxy-1,4-distyrylbenzene

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:81795-78-0 SDS

81795-78-0Relevant articles and documents

A magnetic palladium nickel carbon nanocomposite as a heterogeneous catalyst for the synthesis of distyrylbenzene and biphenyl derivatives

Shafie, Habiballah,Niknam, Khodabakhsh

supporting information, p. 11697 - 11704 (2021/07/12)

A magnetic palladium nickel carbon (Fe3O4@Pd@Ni/C) nanocomposite has been synthesized using a simple one-pot procedure via a hydrothermal approach. Ferric nitrate, palladium acetate, and nickel nitrate were dissolved in water together with glucose, and the mixture was heated in an autoclave. The Fe3O4@Pd@Ni/C nanocomposite was characterized via XRD, TEM, FE-SEM, VSM, EDS, and XPS studies. The catalytic abilities of the Fe3O4@Pd@Ni/C nanocomposite were investigated for the synthesis of distyrylbenzene and 9,10-distyrylanthracene derivatives. This method shows obvious advantages, such as the recyclability of the catalyst, simple experimental operation, and the obtaining of good to excellent yields.

One-pot synthesis and study of spectroscopic properties of oligo(phenylenevinylene)s

Patel, Krupa N.,Bedekar, Ashutosh V.

, p. 6617 - 6621 (2015/11/09)

Two series of OPVs (oligo(phenylenevinylene)), that is, ((1E,1′E)-(2,5-dimethoxy-1,4-phenylene)bis(ethene-2,1-diyl))dibenzene derivatives and 4-((E)-4-((E)-styryl)styryl)pyridine derivatives with different functional groups of varying electronic properties have been synthesized by one-pot Wittig-Heck methodology. The synthesized derivatives have been studied for their optical properties. Amongst them the ((1E,1′E)-(2,5-dimethoxy-1,4-phenylene)bis(ethene-2,1-diyl))dibenzene derivatives with appropriate changes in the end group showed a significant impact on the UV absorption and emission spectra. Particularly NO2-OPV showed distinct solvatochromism in the wavelength range of 218 nm in different solvents. Whereas 4-((E)-4-((E)-styryl)styryl)pyridine derivatives showed clear acidochromism which can be detected visually as well as spectroscopically.

Understanding the unconventional effects of halogenation on the luminescent properties of oligo(phenylene vinylene) molecules

Sun, Chun-Lin,Li, Jun,Geng, Hong-Wei,Li, Hui,Ai, Yong,Wang, Qiang,Pan, Shan-Lin,Zhang, Hao-Li

supporting information, p. 3091 - 3100 (2014/01/06)

It is commonly known that halogenation tends to decrease the luminescence quantum yield of an organic dye, owing to the high electronegativity and heavy-atom effect of the halogen atom. However, based on an investigation of the effects of halogenation on the luminescence of the oligo(phenylene vinylene) (OPV) framework, we demonstrate that halogenation can have positive impact on the solid-state fluorescence and electrochemiluminescence (ECL) properties of OPV derivatives. The chlorinated OPV exhibits a very high solid-state fluorescence quantum yield (91 %), whilst the brominated analogue gives the highest ECL emission intensity. Time-dependent density functional theory calculations, natural bond orbital analysis, and natural transition orbital analysis were performed to assist the understanding of the origin of these positive halogenation effects, which provide insight into the rational design of highly luminescent halogenated organic materials for solid-state devices and ECL applications. Copyright

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