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9-[1,1'-biphenyl]-4-yl-3,3'-Bi-9H-carbazole is a complex organic chemical compound that consists of multiple ring structures, including biphenyl and carbazole groups. It is distinguished by the presence of two nine-membered benzene rings fused on either side to a five-membered nitrogen-containing ring. 9-[1,1'-biphenyl]-4-yl-3,3'-Bi-9H-carbazole, like other carbazole derivatives, may exhibit properties such as fluorescence and electroluminescence, which could make it a valuable material for various applications in the fields of organic light-emitting diodes (OLEDs), photovoltaics, and other optical and electronic devices. The detailed chemical properties of 9-[1,1'-biphenyl]-4-yl-3,3'-Bi-9H-carbazole, including its solubility, melting point, and safety profile, would be contingent upon its exact molecular structure and are likely to be the subject of research in organic chemistry and materials science.

1346669-48-4

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1346669-48-4 Usage

Uses

Used in Organic Light-Emitting Diodes (OLEDs):
9-[1,1'-biphenyl]-4-yl-3,3'-Bi-9H-carbazole is used as a material in OLEDs for its potential fluorescence and electroluminescence properties, which can contribute to the efficiency and performance of these light-emitting devices.
Used in Photovoltaics:
In the photovoltaic industry, 9-[1,1'-biphenyl]-4-yl-3,3'-Bi-9H-carbazole is used as a component in solar cells, leveraging its light-absorbing and charge transport properties to enhance the conversion of sunlight into electricity.
Used in Optical and Electronic Devices:
9-[1,1'-biphenyl]-4-yl-3,3'-Bi-9H-carbazole is used as a component in various optical and electronic devices due to its potential to improve the performance of these technologies, particularly in areas that require materials with specific light-emitting or light-absorbing characteristics.

Check Digit Verification of cas no

The CAS Registry Mumber 1346669-48-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,4,6,6,6 and 9 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1346669-48:
(9*1)+(8*3)+(7*4)+(6*6)+(5*6)+(4*6)+(3*9)+(2*4)+(1*8)=194
194 % 10 = 4
So 1346669-48-4 is a valid CAS Registry Number.

1346669-48-4Relevant articles and documents

Heterocyclic compound, composition including the same, and organic light-emitting device including the heterocyclic compound

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Paragraph 0372-0373, (2020/07/16)

A heterocyclic compound represented by Formula 1, a composition including the same, and an organic light-emitting device including the heterocyclic compound: L1 to L4, L11, a1 to a4, a11, Ar1, Ar2, Ar11, R1 to R7, R11 to R12, b1 to b7, and b11 to b12 are described in the specification.

HETEROCYCLIC COMPOUND, COMPOSITION INCLUDING THE SAME, AND ORGANIC LIGHT-EMITTING DEVICE INCLUDING THE HETEROCYCLIC COMPOUND

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Paragraph 0260-0261, (2019/07/03)

A heterocyclic compound represented by Formula 1: [in-line-formulae](A)n-L, ??Formula 1[/in-line-formulae] wherein, in Formula 1, A, L, and n are the same as described in the specification.

3,3'-bicarbazolyl derivative organic electroluminescent material and application thereof

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Paragraph 0033; 0035; 0036, (2017/07/08)

The invention discloses a 3,3'-bicarbazolyl derivative organic electroluminescent material and an application thereof; the 3,3'-bicarbazolyl derivative organic electroluminescent material has the following molecular structure described in the specificatio

Synthesis method for 9,9'-disubstituent-3,3'-dicarbazyl

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Paragraph 0023; 0024, (2017/08/29)

The invention discloses a synthesis method for 9,9'-disubstituent-3,3'-dicarbazyl, and belongs to the technical field of the organic chemical synthesis. The method comprises the following steps: using 3-boric acid-9-phenylcarbazole as a raw material, and preparing 9-phenyl-3,3'-dicarbazyl under the catalysis of Pd2(dba)3, triphenylphosphine; and preparing a target object by the 9-phenyl-3,3'-dicarbazyl under the catalysis of PdC12(dppf),X-phos. The synthesis method is capable of adjusting the synthetic route, reducing the production of a by-product, improving the yield and reducing the cost. The yield achieves more than 91%. The synthetic route post-treatment of the synthesis method is simple and effective, and is good for industrial production.

Organic compound for optoelectric device and composition for optoelectric device and organic optoelectric device and display device

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Paragraph 0210; 0216; 0217; 0249; 0255; 0256, (2016/10/09)

Disclosed are a first compound for an organic optoelectric device represented by a combination of Chemical Formula I -1 and Chemical Formula I -2 and a composition for an organic optoelectric device including the first compound for an organic optoelectric device and at least one second compound for an organic optoelectric device having a moiety represented by Chemical Formula II, and an organic optoelectric device and a display device including the same. The detailed descriptions of the Chemical Formula I -1, Chemical Formula I -2 and Chemical Formula II are the same as described in the detailed description. According to the invention, the organic optoelectric device with high efficiency and long usage life can be obtained.

COMPOUND FOR ORGANIC OPTOELECTRONIC DEVICE, ORGANIC LIGHT EMITTING DIODE INCLUDING THE SAME AND DISPLAY INCLUDING THE ORGANIC LIGHT EMITTING DIODE

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Paragraph 0261-0263, (2013/03/26)

A compound for an organic optoelectronic device and an organic photoelectric device including the same are provided. A compound for an organic optoelectronic device represented by Chemical Formula 1 is provided to fabricate an organic photoelectric device having excellent electrochemical and thermal stability and life-span characteristics, and high luminous efficiency at a low driving voltage.

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