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713542-04-2

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713542-04-2 Usage

Description

Anthracene, 9,9',9''-(1,3,5-benzenetriyl)tris-, also known as 1,3,5-Tri(anthracen-9-yl)benzene, is a polycyclic aromatic hydrocarbon characterized by its unique molecular structure consisting of three anthracene units connected by a central benzene core. Anthracene, 9,9',9''-(1,3,5-benzenetriyl)trisexhibits distinct chemical and physical properties, making it suitable for various applications in different industries.

Uses

Used in Energy Storage Applications:
Anthracene, 9,9',9''-(1,3,5-benzenetriyl)trisis used as a precursor in the preparation of porous metal-organic polyhedral frameworks. These frameworks are employed in methane storage due to their high surface area, porosity, and stability, offering an efficient solution for natural gas storage and transportation.
Used in Electronics Industry:
In the electronics industry, Anthracene, 9,9',9''-(1,3,5-benzenetriyl)trisis utilized in the preparation of starburst oligofluorenes, which serve as deep-blue OLED (Organic Light Emitting Diode) emitters. These emitters are crucial for the development of high-performance displays and lighting systems, providing vibrant colors, high contrast, and energy efficiency.

Check Digit Verification of cas no

The CAS Registry Mumber 713542-04-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,1,3,5,4 and 2 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 713542-04:
(8*7)+(7*1)+(6*3)+(5*5)+(4*4)+(3*2)+(2*0)+(1*4)=132
132 % 10 = 2
So 713542-04-2 is a valid CAS Registry Number.

713542-04-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 9-[3,5-di(anthracen-9-yl)phenyl]anthracene

1.2 Other means of identification

Product number -
Other names Anthracene,9,9',9''-(1,3,5-benzenetriyl)tris

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:713542-04-2 SDS

713542-04-2Downstream Products

713542-04-2Relevant articles and documents

Porous Metal-Organic Polyhedral Frameworks with Optimal Molecular Dynamics and Pore Geometry for Methane Storage

Yan, Yong,Kolokolov, Daniil I.,Da Silva, Ivan,Stepanov, Alexander G.,Blake, Alexander J.,Dailly, Anne,Manuel, Pascal,Tang, Chiu C.,Yang, Sihai,Schr?der, Martin

, p. 13349 - 13360 (2017)

Natural gas (methane, CH4) is widely considered as a promising energy carrier for mobile applications. Maximizing the storage capacity is the primary goal for the design of future storage media. Here we report the CH4 storage properties in a family of isostructural (3,24)-connected porous materials, MFM-112a, MFM-115a, and MFM-132a, with different linker backbone functionalization. Both MFM-112a and MFM-115a show excellent CH4 uptakes of 236 and 256 cm3 (STP) cm-3 (v/v) at 80 bar and room temperature, respectively. Significantly, MFM-115a displays an exceptionally high deliverable CH4 capacity of 208 v/v between 5 and 80 bar at room temperature, making it among the best performing metal-organic frameworks for CH4 storage. We also synthesized the partially deuterated versions of the above materials and applied solid-state 2H NMR spectroscopy to show that these three frameworks contain molecular rotors that exhibit motion in fast, medium, and slow regimes, respectively. In situ neutron powder diffraction studies on the binding sites for CD4 within MFM-132a and MFM-115a reveal that the primary binding site is located within the small pocket enclosed by the [(Cu2)3(isophthalate)3] window and three anthracene/phenyl panels. The open Cu(II) sites are the secondary/tertiary adsorption sites in these structures. Thus, we obtained direct experimental evidence showing that a tight cavity can generate a stronger binding affinity to gas molecules than open metal sites. Solid-state 2H NMR spectroscopy and neutron diffraction studies reveal that it is the combination of optimal molecular dynamics, pore geometry and size, and favorable binding sites that leads to the exceptional and different methane uptakes in these materials.

Direct Transformation of Esters into Arenes with 1,5-Bifunctional Organomagnesium Reagents

Link, Achim,Fischer, Christian,Sparr, Christof

, p. 12163 - 12166 (2015/10/12)

A direct transformation of carboxylic acid esters into arenes with 1,5-bifunctional organomagnesium reagents is described. This efficient and practical method enables the one-step defunctionalization of various carboxylic acid esters to prepare benzene, anthracene, tetracene, and pentacene derivatives. A double nucleophilic addition of the 1,5-organodimagnesium reagent to the ester is followed by an immediate 1,4-elimination reaction that leads to the direct [5+1] formation of a new aromatic ring.

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