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2,6-dichlorophenanthridine is a synthetic chemical compound with the molecular formula C14H8Cl2N2. It is a derivative of phenanthridine, characterized by the presence of two chlorine atoms at the 2,6 positions. 2,6-dichlorophenanthridine has garnered interest due to its potential antimicrobial, antifungal, and anticancer properties, as well as its applications in the development of fluorescent dyes and as a reagent in organic synthesis. The unique chemical structure and properties of 2,6-dichlorophenanthridine contribute to its versatility, making it a compound with potential applications across various fields.

38052-81-2

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38052-81-2 Usage

Uses

Used in Antimicrobial Applications:
2,6-dichlorophenanthridine is used as an antimicrobial agent for its ability to inhibit the growth of various microorganisms. Its effectiveness in this application is attributed to its chemical structure, which allows it to interfere with essential cellular processes in bacteria and other pathogens.
Used in Antifungal Applications:
In the field of antifungal treatment, 2,6-dichlorophenanthridine is used as an antifungal agent to combat fungal infections. Its action is believed to disrupt the normal functioning of fungal cells, thereby preventing their growth and spread.
Used in Anticancer Applications:
2,6-dichlorophenanthridine is used as an anticancer agent, where it has been studied for its potential to inhibit the growth of cancer cells. 2,6-dichlorophenanthridine may target specific pathways or mechanisms within cancer cells, thereby exerting a therapeutic effect.
Used in Fluorescent Dye Development:
2,6-dichlorophenanthridine is used as a component in the development of fluorescent dyes. Its chemical properties contribute to the dye's fluorescence, making it a valuable tool in various scientific and industrial applications, such as bioimaging and diagnostics.
Used in Organic Synthesis:
In the realm of organic synthesis, 2,6-dichlorophenanthridine is used as a reagent. Its unique structure allows it to participate in a variety of chemical reactions, facilitating the synthesis of complex organic molecules and compounds. This makes it a valuable asset in the field of chemistry, particularly in the development of new pharmaceuticals and materials.

Check Digit Verification of cas no

The CAS Registry Mumber 38052-81-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,0,5 and 2 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 38052-81:
(7*3)+(6*8)+(5*0)+(4*5)+(3*2)+(2*8)+(1*1)=112
112 % 10 = 2
So 38052-81-2 is a valid CAS Registry Number.

38052-81-2SDS

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 2,6-dichlorophenanthridine

1.2 Other means of identification

Product number -
Other names Phenanthridine,2,6-dichloro

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:38052-81-2 SDS

38052-81-2Downstream Products

38052-81-2Relevant academic research and scientific papers

Synthesis and structure-affinity relationships of selective high-affinity 5-HT4 receptor antagonists: Application to the design of new potential single photon emission computed tomography tracers

Dubost, Emmanuelle,Dumas, Noé,Fossey, Christine,Magnelli, Rosa,Butt-Gueulle, Sabrina,Ballandonne, Céline,Caignard, Daniel H.,Dulin, Fabienne,Sopkova De-Oliveira Santos, Jana,Millet, Philippe,Charnay, Yves,Rault, Sylvain,Cailly, Thomas,Fabis, Frederic

, p. 9693 - 9707 (2013/01/16)

The work described herein aims at finding new potential ligands for the brain imaging of 5-HT4 receptors (5-HT4Rs) using single-photon emission computed tomography (SPECT). Starting from the nonsubstituted phenanthridine compound 4a,

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