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12H-[1]benzothieno[2,3-a]carbazole is a chemical compound that belongs to the family of benzothienocarbazoles, which are polycyclic aromatic compounds containing a benzothieno[2,3-a]carbazole moiety. As a member of this family, it may exhibit properties such as fluorescence, intercalation with other substances, or act as a precursor to other compounds, which are commonly associated with compounds of this family. However, the exact properties and potential applications of this specific compound are not extensively studied or reported in literature, indicating its relative obscurity in scientific research. Due to its nature as a polycyclic aromatic compound, it is important to handle 12H-[1]benzothieno[2,3-a]carbazole with care, as it may pose health risks.

222-21-9

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222-21-9 Usage

Uses

Due to the limited information available on 12H-[1]benzothieno[2,3-a]carbazole, its specific applications are not well-defined. However, based on the general properties of benzothienocarbazoles, it can be hypothesized that it may be used in the following ways:
Used in Research and Development:
12H-[1]benzothieno[2,3-a]carbazole could be used as a research compound for studying the properties and potential applications of benzothienocarbazoles. Its use in this context would be for the purpose of advancing scientific understanding and exploring new avenues for its application.
Used in Chemical Synthesis:
As a polycyclic aromatic compound, 12H-[1]benzothieno[2,3-a]carbazole may serve as a precursor or intermediate in the synthesis of other compounds. Its use in this context would be for the purpose of creating new chemical entities with potential applications in various industries.
Used in Material Science:
The potential fluorescence or intercalation properties of 12H-[1]benzothieno[2,3-a]carbazole could make it a candidate for use in material science, particularly in the development of new materials with unique optical or electronic properties. Its use in this context would be for the purpose of enhancing material performance and functionality.

Check Digit Verification of cas no

The CAS Registry Mumber 222-21-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,2 and 2 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 222-21:
(5*2)+(4*2)+(3*2)+(2*2)+(1*1)=29
29 % 10 = 9
So 222-21-9 is a valid CAS Registry Number.

222-21-9Downstream Products

222-21-9Relevant academic research and scientific papers

Synthesis of pentacyclic heteroaromatic systems related to indolocarbazoles alkaloids

Royer, Herve,Joseph, Delphine,Prim, Damien,Kirsch, Gilbert

, p. 1239 - 1251 (1998)

A direct access to pentacyclic molecules via Fischer Indole Synthesis starting from tricyclic ketones is described.

COMPOUND FOR ORGANIC OPTOELECTRONIC DEVICE, COMPOSITION FOR ORGANIC OPTOELECTRONIC DEVICE, ORGANIC OPTOELECTRONIC DEVICE AND DISPLAY DEVICE

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Paragraph 0236-0240, (2022/01/20)

The present invention relates to a compound for an organic optoelectronic device, a composition for the organic optoelectronic device, the organic optoelectronic device, and a display device. Specifically disclosed are the compound for the organic optoelectronic device represented by Chemical Formula 1, the composition for the organic optoelectronic device including the compound, the organic optoelectronic device, and the display device. The detailed information of the chemical formula 1 is defined in the specification.

Cascade annulative π-extension for the rapid construction of carbazole based polyaromatic hydrocarbons

Banerjee, Ankush,Ghosh, Meghna,Kundu, Samrat,Maji, Modhu Sudan,Pal, Shyam Chand

supporting information, p. 5762 - 5765 (2021/06/16)

A Br?nsted acid catalyzed cascade benzannulation strategy for the one-pot synthesis of densely populated poly-aryl benzo[a]carbazole architectures is disclosed from easily affordable fundamental commodities. The efficacy of this technique was further validated via the concise synthesis of structurally unique carbazole based poly-aromatic hydrocarbons. Furthermore, the photo-physical properties of the synthesized compounds are thoroughly investigated.

Composition of matter for use in organic light-emitting diodes

-

, (2021/01/20)

The present disclosure relates to compounds of formula (I) or formula (II) as compounds capable of emitting delayed fluorescence and uses of these compounds in organic light-emitting diodes.

Compounds and application thereof

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Paragraph 0070-0071; 0073, (2020/02/20)

The invention discloses novel compounds and an application thereof. The compounds are represented by a formula (1-1) or a formula (1-2) shown in the description, wherein Z is one selected from the group consisting of O, S, NR, and CR'R''; Y1-Y12 is select

COMPOUND FOR ORGANIC ELECTRIC ELEMENT AND ORGANIC ELECTRIC DEVICE COMPRISING THE SAME

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Paragraph 0363-0365; 0368-0369; 0396; 0398; 0401, (2020/11/28)

The present invention relates to a compound for an organic electronic element and an organic electronic element using the same. To the present invention, an organic electronic element having high luminous efficiency, low driving voltage, and high heat resistance can be provided and the color purity and lifetime of the organic electronic element can be improved. (by machine translation)

Tandem Oxidative Ring-Opening/Cyclization Reaction in Seconds in Open Atmosphere for the Synthesis of 1-Tetralones in Water-Acetonitrile

Fang, Jingxian,Li, Lesong,Yang, Chu,Chen, Jinping,Deng, Guo-Jun,Gong, Hang

, (2018/11/23)

A mild and practical tandem oxidative ring-opening/cyclization reaction mediated by Ce4+ for the synthesis of 1-tetralones is presented. This rapid transformation was completed within 30 s and conducted in an open reactor at 0 °C in a water-acetonitrile mixture. Various cyclobutanol derivatives are transformed into desired products in good to high yields, and this reaction can be easily scaled up to the gram scale.

Tandem Oxidative Ring-Opening/Cyclization Reaction in Seconds in Open Atmosphere for the Synthesis of 1-Tetralones in Water-Acetonitrile

Fang, Jingxian,Li, Lesong,Yang, Chu,Chen, Jinping,Deng, Guo-Jun,Gong, Hang

, p. 7308 - 7311 (2018/11/25)

A mild and practical tandem oxidative ring-opening/cyclization reaction mediated by Ce4+ for the synthesis of 1-tetralones is presented. This rapid transformation was completed within 30 s and conducted in an open reactor at 0 °C in a water-acetonitrile mixture. Various cyclobutanol derivatives are transformed into desired products in good to high yields, and this reaction can be easily scaled up to the gram scale.

A pyrimidine derivatives and application thereof (by machine translation)

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Paragraph 0035; 0047; 0052; 0053, (2018/07/30)

The invention discloses a pyrimidine derivative and its application, the pyrimidine derivatives having the following -like type (I) indicated by the structure; wherein said R1 , R2 , R3 Are selected from the carbon atom number is 1 - 60 alkyl, substituted and non-substituted aromatic heterocyclic radical, and substituted and non-substituted aromatic ring in base of any one group. The invention through the pyrimidine derivatives key chemical structure and the like is improved, and the pyrimidine derivatives as material is applied to the electro-luminescent layer in the organic electroluminescent device, compared with the prior art can effectively solve the organic electroluminescent device in blue light material of poor stability, low efficiency and the like. (by machine translation)

Compound containing a 5-membered heterocycle and organic light-emitting diode using same, and terminal for same

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Page/Page column 47; 48, (2018/07/29)

Disclosed are a novel-structural compound including a 5-membered heterocycle, an organic electronic device using the same, and a terminal thereof.

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