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3-ACETAMIDOACRIDINE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

23043-50-7

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23043-50-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 23043-50-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,0,4 and 3 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 23043-50:
(7*2)+(6*3)+(5*0)+(4*4)+(3*3)+(2*5)+(1*0)=67
67 % 10 = 7
So 23043-50-7 is a valid CAS Registry Number.
InChI:InChI=1/C15H12N2O/c1-10(18)16-13-6-7-15-12(9-13)8-11-4-2-3-5-14(11)17-15/h2-9H,1H3,(H,16,18)

23043-50-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-acridin-3-ylacetamide

1.2 Other means of identification

Product number -
Other names Acetamide,N-3-acridinyl

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:23043-50-7 SDS

23043-50-7Relevant academic research and scientific papers

Facile synthesis of unsymmetrical acridines and phenazines by a Rh(III)-catalyzed amination/cyclization/aromatization cascade

Lian, Yajing,Hummel, Joshua R.,Bergman, Robert G.,Ellman, Jonathan A.

supporting information, p. 12548 - 12551 (2013/09/23)

We report formal [3 + 3] annulations of aromatic azides with aromatic imines and azobenzenes to give acridines and phenazines, respectively. These transformations proceed through a cascade process of Rh(III)-catalyzed amination followed by intramolecular electrophilic aromatic substitution and aromatization. Acridines can be directly prepared from aromatic aldehydes by in situ imine formation using catalytic benzylamine.

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