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Benzene, 1,4-bis[2-(4-nitrophenyl)ethenyl]-, also known as 1,4-bis(4-nitrophenyl)-2-buten-1-ene or 1,4-di(4-nitrophenyl)butadiene, is an organic compound with the molecular formula C18H14N2O4. It is a yellow crystalline solid that is soluble in organic solvents such as ethanol and acetone. Benzene, 1,4-bis[2-(4-nitrophenyl)ethenyl]- is characterized by its benzene core with two 4-nitrophenyl groups attached to the 1 and 4 positions, each connected to a butadiene chain. It is used in the synthesis of various organic compounds and as a chemical intermediate in the production of dyes and pharmaceuticals. Due to its nitro groups, it can be hazardous and should be handled with care, as it may pose risks to human health and the environment.

3547-02-2

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3547-02-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3547-02-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,4 and 7 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3547-02:
(6*3)+(5*5)+(4*4)+(3*7)+(2*0)+(1*2)=82
82 % 10 = 2
So 3547-02-2 is a valid CAS Registry Number.

3547-02-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4-bis[2-(4-nitrophenyl)ethenyl]benzene

1.2 Other means of identification

Product number -
Other names -

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

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More Details:3547-02-2 SDS

3547-02-2Relevant academic research and scientific papers

Synthesis of some new distyrylbenzene derivatives using immobilized Pd on an NHC-functionalized MIL-101(Cr) catalyst: photophysical property evaluation, DFT and TD-DFT calculations

Niknam, Esmaeil,Mahmoodi, Ali,Panahi, Farhad,Heydari Dokoohaki, Maryam,Zolghadr, Amin Reza,Khalafi-Nezhad, Ali

, p. 12374 - 12380 (2021/04/07)

In this study the catalytic application of a heterogeneous Pd-catalyst system based on metal organic framework [Pd-NHC-MIL-101(Cr)] was investigated in the synthesis of distyrylbenzene derivatives using the Heck reaction. The Pd-NHC-MIL-101(Cr) catalyst s

Comparison of 1,4-distyrylfluorene and 1,4-distyrylbenzene analogues: Synthesis, structure, electrochemistry and photophysics

Laughlin, Brynna J.,Duniho, Tyler L.,El Homsi, Samantha J.,Levy, Benjamin E.,Deligonul, Nihal,Gaffen, Joshua R.,Protasiewicz, John D.,Tennyson, Andrew G.,Smith, Rhett C.

, p. 5425 - 5434 (2013/09/02)

A series of nine 1,4-distyrylfluorene derivatives (2) functionalized with substituents of variable electron-donating or -accepting capabilities was synthesised. The photophysical properties of the molecules were investigated, including UV/vis absorption,

One-pot synthesis of stilbenes by dehydrohalogenation-Heck olefination and multicomponent Wittig-Heck reaction

Saiyed, Akeel S.,Bedekar, Ashutosh V.

scheme or table, p. 6227 - 6231 (2011/01/04)

A variant of olefination reaction involving in situ generation of styrene by either one-pot dehydrohalogenation-Heck or one-pot multicomponent Wittig-Heck reaction is developed.

Application of Phase-Transfer Catalysis to the Synthesis of Mono- and Bis-stilbenes and Styryls

Lokhande, S. B.,Rangnekar, D. W.

, p. 485 - 488 (2007/10/02)

A novel and convenient method has been developed for the synthesis of substituted stilbenes by the condensation of active methyl group in suitably substituted toluenes with aromatic aldehydes in aq. medium at room temperature using benzyltriethylammonium chloride as a phase-transfer catalyst.This method has also been applied for the preparation of heterocyclic styryls and extended to the synthesis of bis-stilbenes and bis-styryls using aromatic dialdehydes in place of monoaldehydes.A comparison of the results shows that the present method is superior to the conventional methods in many respects.

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