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Phenazine, 1,3-dimethyl- (7CI,8CI) is a chemical compound with the molecular formula C12H10N2. It is a derivative of phenazine, which is a nitrogen-containing heterocyclic compound with a tricyclic structure consisting of two benzene rings fused to a diazine ring. The 1,3-dimethyl substitution refers to the presence of two methyl groups attached to the phenazine core, specifically at the 1st and 3rd positions. Phenazine, 1,3-dimethyl- (7CI,8CI) is known for its various biological activities, such as antimicrobial and antitumor properties, and is used in research and pharmaceutical applications. It is important to note that handling and usage of this chemical should be done with caution, as it may have potential health risks and environmental impacts.

6479-89-6

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6479-89-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6479-89-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,7 and 9 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6479-89:
(6*6)+(5*4)+(4*7)+(3*9)+(2*8)+(1*9)=136
136 % 10 = 6
So 6479-89-6 is a valid CAS Registry Number.

6479-89-6SDS

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 1,3-dimethylphenazine

1.2 Other means of identification

Product number -
Other names 1,3-Dimethyl-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:6479-89-6 SDS

6479-89-6Downstream Products

6479-89-6Relevant academic research and scientific papers

Rhodium-Catalyzed Reaction of Azobenzenes and Nitrosoarenes toward Phenazines

Xiao, Yan,Wu, Xiaopeng,Wang, Hepan,Sun, Song,Yu, Jin-Tao,Cheng, Jiang

, p. 2565 - 2568 (2019/04/30)

A rhodium-catalyzed annulative reaction between azobenzenes and nitrosoarenes has been developed, leading to a series of phenazines in moderate to good yields. This procedure proceeds with sequential chelation-assisted addition of aryl C-H to nitrosoarenes and ring closure by electrophilic attack of azo group to aryl. During this transformation, the azo group served as not only a traceless directing group but also a building block in the final products.

Synthesis of phenazines by Cu-catalyzed homocoupling of 2-halogen anilines in water

Yu, Lintao,Zhou, Xiangge,Wu, Di,Xiang, Haifeng

supporting information; experimental part, p. 75 - 78 (2012/04/17)

Phenazines are synthesized by Cu-catalyzed homocoupling of 2-iodoanilines or 2-bromoanilines in water in moderate to excellent yields up to 85%.

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