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Benz[b]acridine is a polycyclic aromatic hydrocarbon (PAH) with the chemical formula C19H15N. It is a tricyclic compound consisting of a benzene ring fused to an acridine ring, which is itself a fused polycyclic structure containing two additional six-membered rings. Benz[b]acridine is known for its potential mutagenicity and carcinogenicity, as it can interact with DNA and cause mutations. Due to its hazardous properties, it is not used commercially and is primarily of interest in toxicological and environmental studies. The compound is also a byproduct of certain industrial processes and can be found in polluted environments, such as those affected by combustion and pyrolysis activities.

257-89-6

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257-89-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 257-89-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,5 and 7 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 257-89:
(5*2)+(4*5)+(3*7)+(2*8)+(1*9)=76
76 % 10 = 6
So 257-89-6 is a valid CAS Registry Number.
InChI:InChI=1/C17H11N/c1-2-6-13-11-17-15(9-12(13)5-1)10-14-7-3-4-8-16(14)18-17/h1-11H

257-89-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name benzo[b]acridine

1.2 Other means of identification

Product number -
Other names 5-Azanaphthacene

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:257-89-6 SDS

257-89-6Downstream Products

257-89-6Relevant academic research and scientific papers

Synthesis and characterization of oxadisilole-fused acridines, dioxatrisilole-fused acridines and benzo[b]acridines

Zhang, Jie,Chen, Yali,Chen, Xuanming,Zheng, Xiaoxing,Cao, Weiguo,Chen, Jie,Zhang, Min

, p. 5820 - 5827 (2014)

Oxadisilole-fused acridines, dioxatrisilole-fused acridines and benzo[b]acridines were synthesized through nucleophilic additions and aromatization reactions of arynes with 2-aminoaryl ketones or 2-aminoaryl aldehydes in good yields at room temperature. T

Copper-Catalyzed N,N-Diarylation of Amides for the Construction of 9,10-Dihydroacridine Structure and Applications in the Synthesis of Diverse Nitrogen-Embedded Polyacenes

Tan, Mei-Ling,Tong, Shuo,Hou, Sheng-Kai,You, Jingsong,Wang, Mei-Xiang

, p. 5417 - 5422 (2020/07/08)

We reported herein CuI/DMEDA catalyzed N,N-diarylation reaction of amides with various di(o-bromoaryl)methanes to produce diverse 9,10-dihydroacridine derivatives. The resulting 9,10-dihydroacridine derivatives were oxidized selectively under mild conditions to afford acridine, acridinone, and acridinium derivatives. The copper-catalyzed N,N-diarylation reaction coupled with oxidative aromatization reaction enabled the facile construction of nitrogen atom-embedded tetracenes and pentacenes of different ortho-fused patterns. The luminescence properties, especially the effect of fusion pattern on fluorescence emission of acquired N-polycenes, were also demonstrated.

N-arylation of isatins

-

, (2008/06/13)

A process for the N-arylation of isatins with organo bismuth reagents is disclosed.

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