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3-Chloro-10-phenylacridin-9(10H)-one is a chemical compound with the molecular formula C17H11ClN2O and a molecular weight of 294.73 g/mol. It is a derivative of acridinone, a heterocyclic compound with a tricyclic structure consisting of two benzene rings fused to a pyridine ring. The compound is characterized by the presence of a chlorine atom at the 3-position and a phenyl group at the 10-position. It is a white to off-white crystalline solid and is soluble in organic solvents such as ethanol, methanol, and acetone. 3-Chloro-10-phenylacridin-9(10H)-one has potential applications in the field of pharmaceuticals and organic synthesis, particularly as an intermediate in the synthesis of various acridine-based compounds with potential biological activities.

5472-22-0

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5472-22-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5472-22-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,7 and 2 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5472-22:
(6*5)+(5*4)+(4*7)+(3*2)+(2*2)+(1*2)=90
90 % 10 = 0
So 5472-22-0 is a valid CAS Registry Number.

5472-22-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-chloro-10-phenylacridin-9-one

1.2 Other means of identification

Product number -
Other names 3-Chlor-10-phenyl-10H-acridin-9-on

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:5472-22-0 SDS

5472-22-0Downstream Products

5472-22-0Relevant academic research and scientific papers

Copper-catalyzed synthesis of N-aryl acridones from 2-amino benzophenones and aryl boronic acids via sequential double oxidative C–N coupling

He, Yang,Xu, Liang,Zhang, Jinli,Wei, Yu

, (2019/12/27)

Pot-economic synthesis of N-aryl acridones was performed with 2-aminobenzophenones and aryl boronic acids as starting materials. Cu-catalyzed chelation-assisted oxidative C–N cross-coupling reactions were well merged with the following intra-molecular oxidative dehydrogenative C–H amination reactions under an air atmosphere. The use of reagent capsules can further resolve the compatibility problem of reagents and simplify the operational process, providing a more straightforward access to the target products.

COMPOUND HAVING DOUBLE SPIRO STRUCTURE AND ORGANIC LIGHT EMITTING DEVICE COMPRISING THE SAME

-

Paragraph 0253-0256, (2017/07/26)

The present specification provides a double spiro-structured compound and an organic light emitting device comprising the same. The compound described in the present specification can be used as a material for hole injection, hole transporting, hole injection and hole transporting, light emitting, electron transporting, or electron injection.COPYRIGHT KIPO 2017

Copper-catalyzed intramolecular direct amination of sp2 C-H bonds for the synthesis of N-aryl acridones

Zhou, Wang,Liu, Yong,Yang, Youqing,Deng, Guo-Jun

supporting information, p. 10678 - 10680 (2012/11/07)

A copper-catalyzed approach for the synthesis of N-aryl acridones via sp2 C-H bond amination using air as oxidant under neutral conditions is disclosed. This reaction not only provides a complementary method for synthesizing medicinally important acridones, but also offers a new strategy for sp2 C-H bond amination.

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