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1-Phenylphenazine is an organic compound with the chemical formula C16H11N and a molecular weight of 217.27 g/mol. It is a derivative of phenazine, a heterocyclic aromatic compound consisting of two fused benzene rings with two nitrogen atoms in the ring. The phenyl group is attached to the nitrogen atom at the 1-position, giving the compound its name. 1-Phenylphenazine is a yellow crystalline solid that is soluble in organic solvents and exhibits fluorescence properties. It has potential applications in the fields of organic synthesis, pharmaceuticals, and materials science, particularly as a building block for the development of new compounds with unique electronic and optical properties.

3225-16-9

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3225-16-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3225-16-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,2 and 5 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3225-16:
(6*3)+(5*2)+(4*2)+(3*5)+(2*1)+(1*6)=59
59 % 10 = 9
So 3225-16-9 is a valid CAS Registry Number.

3225-16-9Relevant academic research and scientific papers

An umpolung strategy for rapid access to thermally activated delayed fluorescence (TADF) materials based on phenazine

Cheng, Hu,Guo, Qiang,Lan, Jingbo,Ran, Chunhao,Wu, Di,Zhang, Huaxing

, p. 1581 - 1584 (2022/02/10)

Herein, Ag(I)-promoted regioselective intramolecular radical nucleophilic addition/rearrangement of 2-aryl diazaboroles has been accomplished for the first time to construct phenazine structures. This protocol is an umpolung strategy based on the classical electrophilic mechanism, and therefore, a reversed regioselectivity was observed, which provides an opportunity to prepare sterically hindered phenazines. The resulting thermally activated delayed fluorescence (TADF) materials based on phenazine exhibit emission bands from green to red with high quantum yields and moderate fluorescence lifetimes as solid films.

Synthesis of 1-substituted phenazines as novel antichlamydial agents

Bao, Xiao-Feng,Jiang, He,Liu, Zi-Yi,Xie, Wen-Xia,Zhao, Yu,Zhu, Li,Zhu, Yi-Xin

, (2021/10/21)

A novel series of 1-substituted phenazines 4a-4l were designed and synthesized via Palladium-catalyzed reactions from 1-phenazine trifluoromethanesulfonate. These phenazines showed antichlamydial activity with IC50 values from 1 to 10 μM. Among them, compounds 4c and 4i exhibited the best antichlamydial activity with IC50 values from 2.06 to 2.74 μM without apparent cytotoxicity to host cells.

PHENAZINE-BASED COMPOUND AND ORGANIC LIGHT EMITTING DEVICE COMPRISING THE SAME

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Paragraph 0073-0074; 0117-0118; 0154-0155, (2016/10/08)

The present invention refers to including and compound phenacy relates to organic light emitting device. (by machine translation)

Rh(NHC)-catalyzed direct and selective arylation of quinolines at the 8-position

Kwak, Jaesung,Kim, Min,Chang, Sukbok

supporting information; experimental part, p. 3780 - 3783 (2011/05/05)

A new catalytic protocol for the regioselective direct arylation of quinoline derivatives at the 8-position has been developed. The reaction is catalyzed by a Rh(NHC) system, and the choice of the NHC ligand was most important for achieving high reactivit

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