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9-(4-azidophenyl)-3,6-di-tert-butyl-9H-carbazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1379822-12-4

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1379822-12-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1379822-12-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,9,8,2 and 2 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1379822-12:
(9*1)+(8*3)+(7*7)+(6*9)+(5*8)+(4*2)+(3*2)+(2*1)+(1*2)=194
194 % 10 = 4
So 1379822-12-4 is a valid CAS Registry Number.

1379822-12-4Downstream Products

1379822-12-4Relevant academic research and scientific papers

Efficient and straightforward click synthesis of structurally related dendritic triazoles

Mangione,Spanevello,Anzardi

, p. 47681 - 47688 (2017/10/23)

A simple, rapid and efficient copper-catalyzed 1,3-dipolar cycloaddition reaction is described for the synthesis of a novel family of twelve triazolic dendrimers structurally related. The products were the result of the click reaction of three cores and four different azides in tetrahydrofuran applying a homogeneous copper catalysis. The reaction intermediates and products were obtained in very good to excellent yields using straightforward and simple work-up procedures. This new family of compounds contain electroactive moieties such as carbazole and triphenylamine which may turn them into excellent candidates for the development of optoelectronic organic materials.

Ruthenium(II) photosensitizers of tridentate click-derived cyclometalating ligands: A joint experimental and computational study

Schulze, Benjamin,Escudero, Daniel,Friebe, Christian,Siebert, Ronald,Goerls, Helmar,Sinn, Stephan,Thomas, Martin,Mai, Sebastian,Popp, Juergen,Dietzek, Benjamin,Gonzalez, Leticia,Schubert, Ulrich S.

supporting information; experimental part, p. 4010 - 4025 (2012/06/01)

A systematic series of heteroleptic bis(tridentate)ruthenium(II) complexes of click-derived 1,3-bis(1,2,3-triazol-4-yl)benzene N^C^N-coordinating ligands was synthesized, analyzed by single crystal X-ray diffraction, investigated photophysically and electrochemically, and studied by computational methods. The presented comprehensive characterization allows a more detailed understanding of the radiationless deactivation mechanisms. Furthermore, we provide a fully optimized synthesis and systematic variations towards redox-matched, broadly and intensely absorbing, cyclometalated ruthenium(II) complexes. Most of them show a weak room-temperature emission and a prolonged excited-state lifetime. They display a broad absorption up to 700 nm and high molar extinction coefficients up to 20 000 M-1 cm-1 of the metal-to-ligand charge transfer bands, resulting in a black color. Thus, the complexes reveal great potential for dye-sensitized solar-cell applications. Making sense of sensitization: A systematic series of heteroleptic bis(tridentate) ruthenium(II) complexes of 1,3-bis(1,2,3-triazol-4-yl)benzene N C N-coordinating ligands and 2,2′:6′,2′′-terpyridine was synthesized, analyzed by single-crystal X-ray diffraction, investigated photophysically and electrochemically, and studied by computational methods (see figure) revealing great potential for application in dye-sensitized solar cells. Copyright

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