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N-Octyl-2,7-dibromocarbazole is a chemical compound that is a variant of carbazole, distinguished by its octyl chain and two bromine atoms. It belongs to the class of heterocyclic organic compounds containing a three-ring system. Although specific information about its properties, uses, and safety is limited, its structure suggests potential applications in organic materials, particularly in electronics, due to the semiconducting properties of carbazole compounds.

726169-75-1

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726169-75-1 Usage

Uses

Used in Electronics Industry:
N-Octyl-2,7-dibromocarbazole is used as a semiconducting material for its potential application in electronic devices. The presence of the octyl chain and bromine atoms in its structure may contribute to its electronic properties, making it a candidate for use in organic materials and components.
Used in Organic Materials:
N-Octyl-2,7-dibromocarbazole is used as a component in the development of organic materials, possibly due to its structural characteristics that may enhance the performance of these materials. The exact reasons for its use in this context are not well-defined, but its potential role in improving material properties is a subject for future research.

Check Digit Verification of cas no

The CAS Registry Mumber 726169-75-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,2,6,1,6 and 9 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 726169-75:
(8*7)+(7*2)+(6*6)+(5*1)+(4*6)+(3*9)+(2*7)+(1*5)=181
181 % 10 = 1
So 726169-75-1 is a valid CAS Registry Number.

726169-75-1 Well-known Company Product Price

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  • TCI America

  • (D3935)  2,7-Dibromo-9-n-octylcarbazole  >98.0%(GC)

  • 726169-75-1

  • 200mg

  • 1,150.00CNY

  • Detail

726169-75-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,7-dibromo-9-octylcarbazole

1.2 Other means of identification

Product number -
Other names 2,5-DIMETHYL-7,7,8,8-TETRACYANOQUINODIMETHANE

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:726169-75-1 SDS

726169-75-1Relevant academic research and scientific papers

Star-shaped fluorescent material based on carbazole asymmetric fused ring and preparation method and application of material

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Paragraph 0070-0073; 0081-0084, (2021/04/17)

The invention discloses a star-shaped fluorescent material based on a carbazole asymmetric fused ring as well as a preparation method and application of the star-shaped fluorescent material. The structural formula of the star-shaped fluorescent material based on the carbazole asymmetric fused ring is shown as a formula I. The star-shaped fluorescent material based on the carbazole asymmetric fused ring is a rigid conjugated molecule and has high thermal stability and high fluorescence quantum yield. The space structure can effectively inhibit fluorescence quenching; the star-shaped fluorescent material has high hole and electron injection and transmission capability and has the characteristic of bipolar transmission; the hybrid local charge transfer state characteristic is achieved, the high exciton utilization rate can be obtained, and high efficiency is achieved; the performance of the material is superior to that of a star-shaped fluorescent material based on a carbazole symmetric condensed ring; the star-shaped fluorescent materialhas good solubility, can be dissolved in a common organic solvent, is suitable for solution processing and ink-jet printing, can form a compact film, can be used for preparing a luminescent layer, and is beneficial to preparation of an electroluminescent device with excellent morphology; and when the materiel is used as a light-emitting layer of the device, the external quantum efficiency is 9% or above, and a wide development prospect is achieved.

Structure-activity relationship (SAR) studies on the mutagenic properties of 2,7-diaminofluorene and 2,7-diaminocarbazole derivatives

Kim, Byeong Wook,Lee, Hwa,Keum, Gyochang,Kim, B. Moon

supporting information, (2020/11/27)

We discovered that 2,7-diaminofluorene or 2,7-diaminocarbazole moiety can be employed as a core structure of highly effective NS5A inhibitors that are connected through amide bonds to proline-valine-carbamate motifs. Amide bonds can be easily cleaved via various metabolic pathways upon administration into the body, and metabolites containing 2,7-diaminofluorene and 2,7-diaminocarbazole core structures have been known to be strong mutagens. To avoid the mutagenesis issue of these core structures, we examined various functional groups at the C9 or N9 position of 2,7-diaminofluorene or 2,7-diaminocarbazole, respectively, through the Ames test in TA98 and TA100 mutants of Salmonella typhimurium LT-2. We discovered that, through proper alkyl substitution at the C9 or N9 position, 2,7-diaminofluorene and 2,7-diaminocarbazole moieties can be successfully employed in drug discovery without necessarily causing mutagenicity problems.

Two Anthracene-Based Copolymers as the Hole-Transporting Materials for High-Performance Inverted (p-i-n) Perovskite Solar Cells

Tong, Tong,Tan, Chao,Keller, Tina,Li, Bobo,Zheng, Chaoyue,Scherf, Ullrich,Gao, Deqing,Huang, Wei

, p. 7407 - 7416 (2018/09/27)

Two anthracene-based copolymers, the thiophene-bridged carbazole-anthracene copolymer (abbreviated as PCBZANT) and the thiophene-bridged triphenylamine-anthracene copolymer (abbreviated as PTPAANT), have been developed as the hole-transporting materials (HTMs) for the inverted perovskite solar cells. They were thermally stable with decomposition temperatures of 435 and 420 °C. The High Occupied Molecular Orbitals (HOMO) of -5.15 and -5.24 eV of two copolymers facilitated the hole carriers transfer from the perovskite layer (CH3NH3PbI3, HOMO: -5.4 eV) in contrast to poly(3,4-ethylenedioxythiophene):polystyrenesulfonate (PEDOT:PSS, HOMO: -4.9 eV). The solar cell with PCBZANT (abbreviated as the PCBZANT device) showed the highest power conversion efficiency (PCE) of 15.50%, while the cell with PTPAANT (abbreviated as the PTPAANT device) showed the highest PCE of 14.52%, with increases of 36.2% and 27.6%, respectively, relative to the PEDOT:PSS device. The thorough analysis disclosed that the high performance was mainly ascribed to the enhanced open-circuit voltage (VOC) and short-circuit current density (JSC), being contributed from the efficient hole-carrier extraction, the high hole mobility of two copolymers, and the high-quality perovskite film with large crystal size and less defect. With strong absorption in the range of 350-500 nm, the polymers decreased the destruction of UV-radiation on the perovskite layer as UV-filters and improved the stability of the inverted cells.

CARBAZOLE COMPOUND HAVING ANTI-VIRUS ACTIVITY

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Paragraph 0182; 0183; 0184; 0357; 0358, (2018/03/25)

The present invention relates to a carbazole compound having anti-virus activity, and more particularly, to a novel compound selected from the group of consisting of a carbazole compound which shows excellent anti-proliferative efficacy against hepatitis C virus (HCV), a pharmaceutically acceptable salt thereof, a hydrate thereof, and an isomer thereof; an anti-virus pharmaceutical composition including the novel compound as an active ingredient; a pharmaceutical composition for preventing or treating liver diseases caused by hepatitis C virus; and a method of preparing the novel compound.

Novel A-D-A type small molecules with β-alkynylated BODIPY flanks for bulk heterojunction solar cells

Liao, Junxu,Xu, Yongjun,Zhao, Hongbin,Zong, Qiao,Fang, Yutang

, p. 321 - 333 (2017/07/12)

A serial of novel A-D-A type small molecules with BODIPY linked through alkynyl with various electron donor units such as fluorene, carbazole, benzodithiophene and phenothiazine, namely F-BDP, C-BDP, B-BDP and P-BDP, respectively, were designed and synthe

Ethynyl bridging based A-phi-D-phi-A type BODIPY derivative and preparation method thereof

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Paragraph 0067; 0072, (2017/08/02)

The invention discloses an ethynyl bridging based A-phi-D-phi-A type BODIPY derivative and a preparation method thereof. The A-phi-D-phi-A type BODIPY derivative is prepared by the following steps: grafting ethynyl to groups such as fluorene, carbazole, d

Organic fluorescent sensing material capable of selectively detecting nerve agent, and preparation method and application thereof

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Paragraph 0150; 0151, (2018/01/09)

The invention belongs to the field of organic semiconductor nanomaterials, and concretely relates to an organic fluorescent sensing material capable of selectively detecting a nerve agent, and a preparation method and application thereof. The invention prepares the organic fluorescent sensing material capable of selectively detecting the nerve agent. A series of P type organic fluorescent sensing materials based on carbazole molecules synthesize to form a structure of a carbazole derivative with different side chains through changing side chains of the carbazole molecules and a polymerization degree thereof, and a one-dimensional organic semiconductor nanowire is obtained through a self-assembly method, namely the organic fluorescent sensing material capable of selectively detecting the nerve agent. The nanowire provided by the invention has the characteristics of large specific surface area, more surface porosity and the like, the nerve agent to be detected is favorably adsorbed and diffused on the surface of the nanowire, and a detection limit is greatly reduced. Therefore, the organic fluorescent sensing material provided by the invention can be used as a fluorescence sensor with an excellent performance capable of recognizing the nerve agent.

Organic fluorescence sensing composite material with ultrahigh sensitivity response for explosives as well as preparation and application thereof

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Paragraph 0137; 0139; 0140, (2018/01/04)

The invention relates to an organic fluorescence sensing composite material with ultrahigh sensitivity response for explosives as well as preparation and application thereof. The material is a blended one-dimensional organic semiconductor nanowire obtained by compositing one or more metallorganics complexes based on carbazole molecules and an organic fluorescence sensing material based on a series of carbazole molecules by a self-assembly method; the material has the characteristics of being porous, being large in superficial area, high in fluorescence quantum efficiency, uniform in mixing and the like, is suitable for fluorescence detection for the explosives and is particularly very efficient in detection for trace explosives.

Terpyridine-based donor-acceptor metallo-supramolecular polymers with tunable band gaps: Synthesis and characterization

Li, Fanchao,Hu, Zhiwei,Qiao, Hongbing,Liu, Lin,Hu, Jiawei,Chen, Xuegang,Li, Jie

, p. 142 - 150 (2016/05/19)

Three new building blocks containing the electron-donor fused-ring motifs carbazole, dithienosilole (DTS) and dithienopyrrole (DTP) and the 2,2′:6′,2″-terpyridine electron-acceptor motif were designed and synthesized. Directed by transition metal ions, the self-assembly of the building blocks triggered polymerization to form the corresponding metallo-supramolecular polymers PCzTPY, PSiTPY and PNTPY, respectively. The UV-vis absorption maxima of the building blocks occur at long wavelengths (351, 368 and 430 nm for CzTPY, SiTPY and NTPY, respectively), which arises from intramolecular charge transfer (ICT) transitions. However, the absorption maxima of their corresponding metallo-supramolecular polymers are clearly red-shifted (to 394, 431 and 509 nm for PCzTPY, PSiTPY and PNTPY, respectively), which is caused by the incorporation of the transition metal ion into the backbones of the target polymers. Based on the above strategies, the resulting metallo-polymers exhibit reduced energy gaps, which are 2.07, 1.97 and 1.56 eV for the PCzTPY, PSiTPY and PNTPY metallo-supramolecular polymers, respectively.

A carbazole as nuclear having a butterfly-shaped double-polarity micromolecule the main body material and its preparation method

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Paragraph 0057-0059, (2017/02/28)

The invention discloses a butterfly-shaped bipolar small molecular host material taking carbazole as a core. The structure of the butterfly-shaped bipolar small molecular host material is as follows: electron-donating groups and electron-withdrawing groups are respectively connected to the 2nd, 3rd, 6th and 7th sites of carbazole. The bipolar small molecular host material disclosed by the invention has good electron and hole transporting capability, and can balance carrier transmission, so that more carriers can be effectively compounded in a light-emitting layer and the current efficiency of a device is improved further; meanwhile the butterfly-shaped bipolar small molecular host material also has good solubility, film-forming property and thin film morphological stability. The invention also discloses a preparation method of the bipolar small molecular host material and the preparation method has the advantages of few synthetic steps, easy feasible synthesis and easy purification, thus the preparation method can be put into industrial application favorably.

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