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2,7-dibromopyrene-4,5,9,10-tetraone is a compound with the chemical formula C16H6Br2O4. It is a derivative of pyrene, a polycyclic aromatic hydrocarbon consisting of four fused benzene rings. 2,7-dibromopyrene-4,5,9,10-tetraone features four carbonyl groups and two bromine atoms attached to the pyrene structure, which gives it unique properties for use in various applications.

1204649-68-2

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1204649-68-2 Usage

Uses

Used in Organic Synthesis:
2,7-dibromopyrene-4,5,9,10-tetraone is used as a building block in organic synthesis for creating more complex molecules. Its unique structure and the presence of bromine atoms make it a versatile reagent for a range of chemical reactions.
Used in Chemical Research:
In the field of chemical research, 2,7-dibromopyrene-4,5,9,10-tetraone serves as a valuable compound for studying the properties and reactions of polycyclic aromatic hydrocarbons and their derivatives. Its structure allows researchers to explore potential applications in material science and pharmaceutical development.
Used in the Development of Novel Materials:
Due to its distinct structure, 2,7-dibromopyrene-4,5,9,10-tetraone is used as a starting material for the development of novel materials with specific properties. The integration of bromine atoms can influence the compound's reactivity and stability, making it suitable for various material applications.
Used in Pharmaceutical Research:
2,7-dibromopyrene-4,5,9,10-tetraone's unique structure also makes 2,7-dibromopyrene-4,5,9,10-tetraone a candidate for pharmaceutical research. It can be used as a precursor in the synthesis of new drugs or as a probe to study biological interactions.
However, it is important to note that the compound's toxicity and environmental impact should be carefully considered when working with it, as with any chemical compound. Proper safety measures and disposal methods must be adhered to ensure the well-being of researchers and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 1204649-68-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,4,6,4 and 9 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1204649-68:
(9*1)+(8*2)+(7*0)+(6*4)+(5*6)+(4*4)+(3*9)+(2*6)+(1*8)=142
142 % 10 = 2
So 1204649-68-2 is a valid CAS Registry Number.

1204649-68-2Downstream Products

1204649-68-2Relevant academic research and scientific papers

Synthesis and photovoltaic properties of conjugated D-A copolymers based on thienyl substituted pyrene and diketopyrrolopyrrole for polymer solar cells

Wang, Ning,Bao, Xichang,Yan, Yan,Ouyang, Dan,Sun, Mingliang,Roy,Lee, Chun Sing,Yang, Renqiang

, p. 3198 - 3204 (2014)

A new donor-acceptor conjugated copolymer (PDTPyDPP), comprising 2,7-di-2-thienyl-4,5,9,10-tetrakis(hexyloxy)pyrene as a donor and diketopyrrolopyrrole (DPP) as an acceptor, was synthesized. PDTPyDPP showed good solubility in common organic solvents, broad visible absorption from 300 to 900 nm, and a moderate hole mobility up to 6.3 × 10-3 cm2 V-1 s-1. The power conversion efficiency of the photovoltaic device based on the PDTPyDPP/PC71BM photoactive layer reached 4.43% with 0.66 V of open-circuit voltage (Voc), 10.52 mA cm-2 of short-circuit current (Jsc) and 64.11% of fill factor.

A Highly Ordered Nanoporous, Two-Dimensional Covalent Organic Framework with Modifiable Pores, and Its Application in Water Purification and Ion Sieving

Kuehl, Valerie A.,Yin, Jiashi,Duong, Phuoc H. H.,Mastorovich, Bruce,Newell, Brian,Li-Oakey, Katie Dongmei,Parkinson, Bruce A.,Hoberg, John O.

, p. 18200 - 18207 (2018)

The preparation of membranes with high selectivity based on specific chemical properties such as size and charge would impact the efficiency of the world's energy supply, the production of clean water, and many other separation technologies. We report a flexible synthetic protocol for preparing highly ordered two-dimensional nanoporous polymeric materials (termed covalent organic frameworks or COFs) that allow for placing virtually any function group within the nanopores. We demonstrate that membranes, fabricated with this new family of materials with carboxylated pore walls, are very water permeable, as well as highly charged and size selective.

Optical Effect of Varying Acceptors in Pyrene Donor–Acceptor–Donor Chromophores

Keller, Samantha N.,Bromby, Ashley D.,Sutherland, Todd C.

, p. 3980 - 3985 (2017)

Three donor–acceptor–donor (D–A–D) pyrene chromophores are described and compared by DFT computations. The two properties of low energy photon absorption and low energy electrochemical reduction are demonstrated through a pyrene framework. Altering the electron-acceptor strength of the pyrene core by chemical oxidation or installation of a thiadiazole dioxide heterocycle results in the formation of D–A–D chromophores with absorption bands up to 900 nm and LUMO energy levels of approximately –4.1 eV vs. vacuum.

Electron donors and acceptors based on 2,7-functionalized pyrene-4,5,9,10-tetraone

Kawano, Shin-Ichiro,Baumgarten, Martin,Chercka, Dennis,Enkelmann, Volker,Muellen, Klaus

, p. 5058 - 5060 (2013)

An efficient synthesis of 2,7-dibromo- and diiodo-pyrene(4,5,8,19)- tetraones led to strong donors and acceptors based on pyrene. They are versatile building blocks for conjugated materials and can be further applied in molecular electronics. The Royal Society of Chemistry 2013.

An extended carbonyl-rich conjugated polymer cathode for high-capacity lithium-ion batteries

Zheng, Shibing,Miao, Licheng,Sun, Tianjiang,Li, Lin,Ma, Tao,Bao, Junquan,Tao, Zhanliang,Chen, Jun

, p. 2700 - 2705 (2021)

Organic materials have attracted extensive attention for use in lithium-ion batteries due to the flexible designability of their structures and their high theoretical capacities. However, the high solubilities, low voltages, and poor conductivities of traditional organic materials have impeded their further application. Herein, a novel carbonyl-rich covalent organic polymer (COP), polyphenyl-1,3,5-(pyrene-4,5,9,10-tetraone) (PPh-PTO), was designed and synthesized.In situFourier-transform infrared spectroscopy (FTIR),ex situX-ray photoelectron spectroscopy (XPS), and Raman analysis were used to confirm the carbonyl redox-active centers. Moreover, density functional theory (DFT) calculations were used to verify that the extended conjugated structure can induce electron delocalization and achieve an elevated and slanted voltage plateau in comparison with the pyrene-4,5,9,10-tetraone (PTO) monomer. The extended structure enables PPh-PTO to show a high reversible capacity of 235 mA h g?1at 0.1 A g?1, superior cycling abilities (95% capacity retention after 1400 cycles), and excellent rate performance (94 mA h g?1at 2 A g?1) in lithium-ion batteries. Our work developed a promising strategy for designing high-energy carbonyl-rich covalent organic polymers for energy storage.

Aromatic ring pyrene quinone compound and application thereof

-

, (2021/03/30)

The invention relates to an aromatic ring pyrene quinone compound, a polymer and application thereof. The aromatic ring pyrene quinone compound has a structure shown as a formula (I1), shows excellenthole transport property and stability, can be used as a hole injection layer material in an organic electroluminescent element, and can also be doped in a hole injection layer or a hole transport layer as a doping agent, so that a device can be driven at a low voltage, the electroluminescent efficiency can be improved, and the service life of the device can be prolonged.

Organic compound, mixture and composition and application thereof

-

, (2021/06/02)

The invention relates to an organic compound, a mixture and a composition and an application thereof, and in particular, relates to an application in an organic light-emitting diode. The organic compound disclosed by the invention, represented by a general formula (1), has excellent hole transport property and stability, can be used as a hole injection layer material in an organic electroluminescent element, and can also be used as a dopant to be doped in a hole injection layer or a hole transport layer, so that low-voltage driving can be realized, the electroluminescent efficiency can also be improved, and the device life is prolonged.

Pyrene quinone organic compound and application thereof

-

, (2020/02/17)

The invention relates to a pyrene quinone organic compound shown in a general formula (I) and application thereof. The pyrene quinone organic compound has excellent hole transport properties and stability, can be used as a hole injection layer material in an organic light emitting device and can also be doped in a hole injection layer or a hole transport layer as a dopant so as to be driven by lowvoltage and improve light emitting efficiency and prolong service life of the device.

NOVEL POLYMERS

-

Paragraph 0197, (2014/12/09)

The present invention relates to polymers comprising repeating unit(s) of the formula (I), and their use in electronic devices. The polymers according to the invention have excellent solubility in organic solvents and excellent film-forming properties. In

NOVEL POLYMERS

-

, (2011/07/06)

The present invention relates to polymers comprising repeating unit(s) of the formula (I), and their use in electronic devices. The polymers according to the invention have excellent solubility in organic solvents and excellent film-forming properties. In

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