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9-Anilinoacridine, also known as 9-(4-aminophenyl)acridine, is an organic compound with the chemical formula C17H14N2. It is a derivative of acridine, a tricyclic aromatic compound, and features an aniline group attached to the 9-position of the acridine ring. This yellow crystalline solid is used as an intermediate in the synthesis of various dyes, pharmaceuticals, and agrochemicals. 9-Anilinoacridine is known for its fluorescent properties and has been studied for potential applications in fluorescence sensing and imaging. It is also used in the production of certain azo dyes and as a reagent in chemical analysis. Due to its potential health and environmental risks, handling and disposal of 9-anilinoacridine must be done with proper safety measures.

3340-22-5

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3340-22-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3340-22-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,4 and 0 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3340-22:
(6*3)+(5*3)+(4*4)+(3*0)+(2*2)+(1*2)=55
55 % 10 = 5
So 3340-22-5 is a valid CAS Registry Number.
InChI:InChI=1/C19H14N2/c1-2-8-14(9-3-1)20-19-15-10-4-6-12-17(15)21-18-13-7-5-11-16(18)19/h1-13H,(H,20,21)

3340-22-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-phenylacridin-9-amine

1.2 Other means of identification

Product number -
Other names Acridin-9-yl-phenyl-amin

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:3340-22-5 SDS

3340-22-5Downstream Products

3340-22-5Relevant academic research and scientific papers

Diverse tandem cyclization reactions of o -cyanoanilines and diaryliodonium salts with copper catalyst for the construction of quinazolinimine and acridine scaffolds

Pang, Xinlong,Chen, Chao,Su, Xiang,Li, Ming,Wen, Lirong

supporting information, p. 6228 - 6231 (2015/01/09)

Two cyclization modes are realized to produce different nitrogen-containing heterocycles, i.e.; quinazolin-4(3H)-imines and acridines by assembling o-cyanoanilines and diaryliodonium salts via tandem reaction pathways.

Synthesis and?SAR study of?acridine, 2-methylquinoline and?2-phenylquinazoline analogues as?anti-prion agents

Cope,Mutter,Heal,Pascoe,Brown,Pratt,Chen

, p. 1124 - 1143 (2007/10/03)

Transmissible spongiform encephalopathies (TSEs) are thought to arise from aggregation of a protease resistant protein denoted PrPSc, which is a misfolded isoform of the normal cellular prion protein PrPC. Using virtual high-throughp

Gas-phase cyclisation reactions of 1-(2-arylaminophenyl)alkaniminyl radicals

Leardini, Rino,McNab, Hamish,Nanni, Daniele,Parsons, Simon,Reed, David,Tenan, Anton G.

, p. 1833 - 1838 (2007/10/03)

Flash vacuum pyrolysis (FVP) of the oxime ethers 9-11 at 650°C (10-2-10-3 Torr) gives products such as the nitrile 17, carbazoles 19 and 20 and acridines 18 and 21 derived from the corresponding iminyl radicals 13-15. The mechanism proposed for the formation of the acridines involves a key hydrogen abstraction by the iminyl of the adjacent N-H atom. When this route is blocked by an N-methyl group, as in 12, alternative cyclisations ensue, yielding the dihydroquinazoline 26 (via another hydrogen abstraction process) and the benzimidazole 25 (via an iminyl-imidoyl interconversion).

SPECTRAL AND LUMINESCENT PROPERTIES OF 9-ARYLAMINOACRIDINES

Budyka, M. F.,Fatkulbayanov, R. M.

, p. 1075 - 1080 (2007/10/02)

A study has been made of the influence of electronic and steric factors of the aromatic substituent in 9-arylaminoacridines on the behavior of these compounds when subjected to light quanta or electron impact.It has been shown that the introduction of don

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