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Acridine, 4-methoxy-, also known as 4-methoxyacridine, is an organic compound with the chemical formula C15H12N2O. It is a derivative of the acridine family, characterized by a fused-ring structure consisting of three six-membered rings and one five-membered ring. This yellow crystalline solid is soluble in organic solvents such as ethanol and acetone. 4-Methoxyacridine has various applications, including its use as a fluorescent brightening agent, a chemiluminescent reagent, and a potential anti-cancer agent due to its ability to intercalate DNA. It is also employed as a reagent in analytical chemistry for the detection of certain metal ions. The compound is synthesized by the methylation of 4-hydroxyacridine and is known for its photophysical properties, making it a subject of interest in the field of luminescent materials.

3295-61-2

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3295-61-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3295-61-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,9 and 5 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3295-61:
(6*3)+(5*2)+(4*9)+(3*5)+(2*6)+(1*1)=92
92 % 10 = 2
So 3295-61-2 is a valid CAS Registry Number.

3295-61-2SDS

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 4-methoxyacridine

1.2 Other means of identification

Product number -
Other names 4-methoxy-acridine

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:3295-61-2 SDS

3295-61-2Downstream Products

3295-61-2Relevant academic research and scientific papers

Nickel-Catalyzed Transformations of 2,1-Benzisoxazoles with Organozinc Reagents

Baum, Jonathan S.,Condon, Michael E.,Shook, David A.

, p. 2983 - 2988 (2007/10/02)

A novel transformation of 2,1-benzisoxazoles (anthranils) involving nitrogen-oxygen bond rupture with concomitant nitrogen-carbon bond formation by reaction with aryl-, methyl, or 2-thienylzinc chlorides in the presence of nickel catalyst is described.The products of the reaction are o-(substituted-amino)benzaldehydes and benzophenones, precursors of a series of heterocyclic derivatives, including acridines, quinolones, and the novel 7-chloro-1,3-dihydro-1,5-diphenyl-2H-1,4-benzodiazepin-2-one (21)

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