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13860-45-2

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13860-45-2 Usage

Chemical class

Phenazine

Structure

Central phenazine ring with two methoxy groups attached at the 1 and 4 positions

Applications

Organic electronic devices (OLEDs and OPVs)

Properties

High electron-affinity and good charge transport

Potential uses

Pharmaceutical and biomedical fields

Investigated properties

Antioxidant and anti-inflammatory

Versatility

Applications in various industries, including electronics and healthcare

Check Digit Verification of cas no

The CAS Registry Mumber 13860-45-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,8,6 and 0 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 13860-45:
(7*1)+(6*3)+(5*8)+(4*6)+(3*0)+(2*4)+(1*5)=102
102 % 10 = 2
So 13860-45-2 is a valid CAS Registry Number.

13860-45-2SDS

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 1,4-dimethoxyphenazine

1.2 Other means of identification

Product number -
Other names 1,4-Dimethoxy-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:13860-45-2 SDS

13860-45-2Downstream Products

13860-45-2Relevant articles and documents

-

Slack,Slack

, p. 437 (1947)

-

Potential chemopreventive agents based on the structure of the lead compound 2-bromo-1-hydroxyphenazine, isolated from streptomyces species, strain CNS284

Conda-Sheridan, Martin,Marler, Laura,Park, Eun-Jung,Kondratyuk, Tamara P.,Jermihov, Katherine,Mesecar, Andrew D.,Pezzuto, John M.,Asolkar, Ratnakar N.,Fenical, William,Cushman, Mark

experimental part, p. 8688 - 8699 (2011/02/28)

The isolation of 2-bromo-1-hydroxyphenazine from a marine Streptomyces species, strain CNS284, and its activity against NF-κB, suggested that a short and flexible route for the synthesis of this metabolite and a variety of phenazine analogues should be developed. Numerous phenazines were subsequently prepared and evaluated as inducers of quinone reductase 1 (QR1) and inhibitors of quinone reductase 2 (QR2), NF-κB, and inducible nitric oxide synthase (iNOS). Several of the active phenazine derivatives displayed IC50 values vs QR1 induction and QR2 inhibition in the nanomolar range, suggesting that they may find utility as cancer chemopreventive agents.

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