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6,13-dihydrodibenzo[b,i]phenazine is a polycyclic aromatic compound with a molecular formula C18H12N2. It is a yellow crystalline solid that is insoluble in water but soluble in organic solvents.

10350-06-8

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10350-06-8 Usage

Uses

Used in Organic Electronics:
6,13-dihydrodibenzo[b,i]phenazine is used as a building block for the synthesis of organic semiconductors and light-emitting materials, contributing to the advancement of organic electronics.
Used in Organic Photovoltaic Devices:
6,13-dihydrodibenzo[b,i]phenazine is being studied for its potential use in the development of organic photovoltaic devices, indicating its role in the field of renewable energy.
Used in Medicinal Chemistry:
6,13-dihydrodibenzo[b,i]phenazine has been investigated for its biological activities, including its potential as an antitumor and antimicrobial agent, showcasing its potential in the development of new pharmaceuticals.

Check Digit Verification of cas no

The CAS Registry Mumber 10350-06-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,3,5 and 0 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 10350-06:
(7*1)+(6*0)+(5*3)+(4*5)+(3*0)+(2*0)+(1*6)=48
48 % 10 = 8
So 10350-06-8 is a valid CAS Registry Number.
InChI:InChI=1/C20H14N2/c1-2-6-14-10-18-17(9-13(14)5-1)21-19-11-15-7-3-4-8-16(15)12-20(19)22-18/h1-12,21-22H

10350-06-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 6,13-Dihydrodibenzo(b,i)phenazine

1.2 Other means of identification

Product number -
Other names 6,13-Dihydro-6,13-diazapentacen

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:10350-06-8 SDS

10350-06-8Relevant academic research and scientific papers

Hash-Mark-Shaped Azaacene Tetramers with Axial Chirality

Inoue, Yuki,Sakamaki, Daisuke,Tsutsui, Yusuke,Gon, Masayuki,Chujo, Yoshiki,Seki, Shu

, p. 7152 - 7158 (2018)

The tetramers of azapentacene derivatives with unique hash mark -

Synthesis, assembly, and thin film transistors of dihydrodiazapentacene: An isostructural motif for pentacene

Miao, Qian,Nguyen, Thuc-Quyen,Someya, Takao,Blanchet, Graciela B.,Nuckolls, Colin

, p. 10284 - 10287 (2003)

The study below details the synthesis, assembly, and thin film transistors from dihydrodiazapentacenes. These molecules have the same molecular shape as pentacene but are much easier to prepare and have much greater environmental stability. Thin films made from the dihydrodiazapentacene behave as field effect transistors with mobilities and on/off ratios high enough to be useful in certain applications. X-ray diffraction and AFM experiments on these films show that the molecules stack in layers with their long axis upright from the surface. Some of the derivatives synthesized for this study have unexpectedly high solubility in polar solvents such as DMF and DMSO. The crystal structure from DMF reveals self-assembled channels with each of the aniline functionalities forming a hydrogen bond with solvent. In more nonpolar solvents, the solid-state assembly switches to a herringbone motif characteristic of the linear acenes.

LIGHT-EMITTING MATERIAL FOR ORGANIC ELECTROLUMINESCENT DEVICE, ORGANIC ELECTROLUMINESCENT DEVICE USING SAME, AND MATERIAL FOR ORGANIC ELECTROLUMINESCENT DEVICE

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Paragraph 0163-0165, (2016/10/17)

In the present invention, disclosed are a novel aromatic compound with outstanding light-emitting efficiency and heat stability, a manufacturing method thereof and an organic electronic device including the novel aromatic compound. For this, in the present invention, provided are a ring-formed aromatic compound and a novel aromatic amine derivative denoted by chemical formula 1 for improving performance of the device.COPYRIGHT KIPO 2015

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