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517-45-3

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517-45-3 Usage

Description

9,9'-DIXANTHYLIDENE, also known as 9,9'-bianthryl, is a polycyclic aromatic hydrocarbon with the molecular formula C28H18. It is characterized by two anthryl groups connected by a carbon-carbon double bond, forming a yellow crystalline solid. This chemical compound is known for its high thermal stability and strong fluorescence, making it a valuable component in various scientific and technological applications.

Uses

Used in Biochemical and Analytical Studies:
9,9'-DIXANTHYLIDENE is used as a fluorescent probe for its ability to emit light upon exposure to a light source, which is crucial in various biochemical and analytical studies. Its fluorescence properties allow researchers to track and monitor molecular interactions and processes.
Used in Optoelectronic Materials and Devices:
9,9'-DIXANTHYLIDENE is utilized in the development of optoelectronic materials and devices due to its unique molecular structure and electronic properties. Its strong fluorescence and stability contribute to the performance of organic light-emitting diodes (OLEDs) and organic photovoltaic devices, enhancing their efficiency and reliability.
Used in Organic Light-Emitting Diodes (OLEDs):
In the application industry of OLEDs, 9,9'-DIXANTHYLIDENE is used as a key component to improve the light-emitting efficiency and color quality of the devices. Its incorporation into OLEDs can lead to brighter and more vibrant displays.
Used in Organic Photovoltaic Devices:
9,9'-DIXANTHYLIDENE is employed in organic photovoltaic devices as a component that can enhance the conversion of light into electricity. Its electronic properties and fluorescence characteristics contribute to the overall performance and efficiency of these solar energy conversion systems.
Safety Note:
It is important to handle 9,9'-DIXANTHYLIDENE with care, as it may pose health risks if swallowed, inhaled, or comes into contact with the skin. Proper safety measures should be taken during its use in laboratories and industrial settings to minimize potential hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 517-45-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,1 and 7 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 517-45:
(5*5)+(4*1)+(3*7)+(2*4)+(1*5)=63
63 % 10 = 3
So 517-45-3 is a valid CAS Registry Number.

517-45-3 Well-known Company Product Price

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  • Alfa Aesar

  • (B21730)  9,9'-Dixanthylidene, 98%   

  • 517-45-3

  • 1g

  • 526.0CNY

  • Detail
  • Alfa Aesar

  • (B21730)  9,9'-Dixanthylidene, 98%   

  • 517-45-3

  • 5g

  • 1964.0CNY

  • Detail

517-45-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 9-xanthen-9-ylidenexanthene

1.2 Other means of identification

Product number -
Other names 9-(9H-Xanthen-9-ylidene)-9H-xanthene

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:517-45-3 SDS

517-45-3Relevant articles and documents

Mills,Nyburg

, p. 308,309 (1963)

Locking the phenyl rings of tetraphenylethene step by step: Understanding the mechanism of aggregation-induced emission

Shi, Junqing,Chang, Ning,Li, Cuihong,Luo, Xiaoliang,Liu, Zhengping,Bo, Zhishan,Dong, Yong Qiang,Mei, Ju,Tang, Ben Zhong,Deng, Chunmei

supporting information, p. 10675 - 10677,3 (2020/09/02)

Stepwise locking of phenyl rings of tetraphenylethene increases the emission efficiency of luminogen solutions gradually, thus verifying the restriction of intramolecular rotation (RIR) mechanism of the aggregation induced emission phenomenon. The emissio

Bimolecular formation of radicals by hydrogen transfer, 12: Transfer hydrogenation of p-substituted α-methylstyrenes and of 9-methylenefluorene as a criterion of mechanism

Friebolin, Heike,Roers, Rolf,Ebenhoch, Jochen,Gerst, Matthias,Ruechardt, Christoph

, p. 385 - 389 (2007/10/03)

The uncatalyzed transfer hydrogenation of substituted α-methylstyrenes with 9,10-dihydroanthracene (DHA), xanthene (XAN), or 9,10-dihydroacridine (DHAC) was studied mechanistically. The three hydrogen donors react at very similar rates and with similar activation parameters and with little discrimination between the various substituted styrenes. The kinetic isotope effects are also similar and the solvent effect is small. A hydrogen atom transfer mechanism (retrodisproportionation) is, therefore, preferred to a hydride transfer mechanism. This is supported by the very similar reactivity of the hydrogen transfer reaction of DHA and XAN with 9-methylenefluorene. The product yields in all reactions investigated in this project were >90%. VCH Verlagsgesellschaft mbH, 1997.

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