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3,7-dibromo-10-(4-(hexyloxy)phenyl)-10H-phenothiazine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1403613-83-1

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1403613-83-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1403613-83-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,3,6,1 and 3 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1403613-83:
(9*1)+(8*4)+(7*0)+(6*3)+(5*6)+(4*1)+(3*3)+(2*8)+(1*3)=121
121 % 10 = 1
So 1403613-83-1 is a valid CAS Registry Number.

1403613-83-1Relevant academic research and scientific papers

Structure-Directed Functional Properties of Phenothiazine Brominated Dyes: Morphology and Photophysical and Electrochemical Properties

Bejan, Andrei,Shova, Sergiu,Damaceanu, Mariana-Dana,Simionescu, Bogdan C.,Marin, Luminita

, p. 3716 - 3730 (2016)

A series of nine dyes based on electron-donating phenothiazine core functionalized with various carbonyl containing electron-withdrawing moieties as primary end group and with or without bromine as a second heavy end group were designed and synthesized to generate variable supramolecular architectures with distinct thermotropic, photophysical, and electrochemical properties. The supramolecular architecture of the obtained dyes was studied in detail by single crystal X-ray diffraction and polarized light microscopy, while optoelectronic properties were investigated by UV-vis and photoluminescence spectroscopy and cyclic voltammetry measurements. The phenothiazine dyes emit light from UV to orange domain, depending on the electron-withdrawing substituent, with great quantum yield reaching up to 71% and high color purity. The introduction of the bromine as a second substituent produced a nearly 2-fold increase of the quantum yield, compared with their counterparts. It was settled that this major benefit of the bromine on the improvement of the quantum yield happened because by its presence some molecular orbital interactions were generated. An interesting and challenging achievement was evidenced in the case of the direct connection of the formyl group to the phenothiazine ring when an unexpected planarization of the dye, unknown up to now in the literature, with drastic consequences on the photophysical and electrochemical behavior was attained. It was concluded that there is a close relationship between the nature of the building blocks of the phenothiazine dyes and their ability to promote favorable properties for different optoelectronic applications.

Phenothiazine based co-crystals with enhanced luminescence

Marin, Luminita,Bejan, Andrei,Shova, Sergiu

, (2019/12/30)

A series of binary phenothiazine based co-crystals were designed with the aim to reach materials with improved quantum efficiency in solid state. To this end, a host dibromine functionalized phenothiazine was mixed with a guest formyl based phenothiazine

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