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Benzene, 2-ethenyl-1,3,5-trimethoxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

40243-91-2

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40243-91-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 40243-91-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,2,4 and 3 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 40243-91:
(7*4)+(6*0)+(5*2)+(4*4)+(3*3)+(2*9)+(1*1)=82
82 % 10 = 2
So 40243-91-2 is a valid CAS Registry Number.

40243-91-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-ethenyl-1,3,5-trimethoxybenzene

1.2 Other means of identification

Product number -
Other names 1,3,5-trimethoxy-2-vinylbenzen

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:40243-91-2 SDS

40243-91-2Relevant academic research and scientific papers

The synthesis of atalantrenes B, C and D, styrene-dimers from the seeds of Atalantia monophylla

Nielsen, Alexander J.,Deng, Zirou,McNulty, James

, (2021)

Concise syntheses of three recently reported natural products from Atalantia monophylla are reported. The syntheses required the preparation and careful dimerization of highly electron rich styrenes under acidic conditions. The present work adds to a growing body of evidence that demonstrates that synthetic utility of chiral phosphoric acids in asymmetric reactions using styrene-type compounds.

Photoinduced, copper-catalyzed three components cyanofluoroalkylation of alkenes with fluoroalkyl iodides as fluoroalkylation reagents

Guo, Quanping,Wang, Mengran,Wang, Yanfang,Xu, Zhaoqing,Wang, Rui

supporting information, p. 12317 - 12320 (2017/11/20)

In the past few years, Ru and Ir catalyzed photoredox radical coupling reactions have been widely applied in organic synthesis. In contrast, the applications of Cu catalysts in photoredox organic transformations were limited. We here report the first example of photoinduced, Cu-catalyzed three component cyanofluoroalkylation of alkenes by directly using fluoroalkyl iodides as fluoroalkylation reagents.

Synthesis of ortho/ortho ′-substituted 1,1-diarylethylenes through cross-coupling reactions of sterically encumbered hydrazones and aryl halides

Roche, Maxime,Hamze, Abdallah,Provot, Olivier,Brion, Jean-Daniel,Alami, Mouad

supporting information, p. 445 - 454 (2013/03/13)

The reactivity of sterically hindered N-tosylhydrazones 2 featuring ortho/ortho′-substituents on the aromatic ring with various ortho-, meta-, and para-substituted aryl halides 3 was investigated. To accomplish successfully this challenging coupling, fine-tuning of the reaction conditions were required. The newly established PdCl2(MeCN)2/Xphos/ NaO-t-Bu/F-benzene system in a sealed tube is compatible with a broad spectrum of both coupling partners, regardless of their electronic and steric nature. This protocol has been applied successfully to the synthesis of a xanthene derivative.

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