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Benzo(a)phenazine is a heterocyclic organic compound with the molecular formula C12H8N2. It is a derivative of phenazine, which is a nitrogen-containing aromatic compound. Benzo(a)phenazine is characterized by its deep blue color and is known for its various applications in the chemical industry. It is used as a dye, particularly in the textile industry, and has potential applications in the development of new materials due to its unique electronic properties. Additionally, benzo(a)phenazine has been studied for its potential use in the synthesis of other compounds and as a building block in the creation of more complex molecular structures. Its chemical properties and stability make it an interesting subject for further research and development in the field of organic chemistry.

225-61-6

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225-61-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 225-61-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,2 and 5 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 225-61:
(5*2)+(4*2)+(3*5)+(2*6)+(1*1)=46
46 % 10 = 6
So 225-61-6 is a valid CAS Registry Number.
InChI:InChI=1/C16H10N2/c1-2-6-12-11(5-1)9-10-15-16(12)18-14-8-4-3-7-13(14)17-15/h1-10H

225-61-6SDS

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 Benzo[a]phenazine

1.2 Other means of identification

Product number -
Other names 1.2-Benzo-phenazin

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:225-61-6 SDS

225-61-6Relevant academic research and scientific papers

Oxidative skeletal rearrangement of 1,1′-binaphthalene-2,2′- diamines (BINAMs) via C-C bond cleavage and nitrogen migration: A versatile synthesis of U-shaped azaacenes

Takeda, Youhei,Okazaki, Masato,Minakata, Satoshi

supporting information, p. 10291 - 10294 (2014/08/18)

An oxidative skeletal rearrangement of 1,1′-binaphthalene-2,2′- diamines (BINAMs) that involves the cleavage of a strong C-C single bond of the binaphthalene unit and the nitrogen migration has been discovered. The unprecedented rearrangement enables access to a series of U-shaped azaacenes otherwise difficult to prepare in a selective manner by classical methods. Moreover, physicochemical properties of the unique azaacenes have been comprehensively investigated. This journal is the Partner Organisations 2014.

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