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3,4-Dihydrobenz[a]anthracen-1(2H)-one, a polycyclic aromatic ketone compound with the chemical formula C18H12O, is a derivative of benz[a]anthracene and belongs to the family of polycyclic aromatic hydrocarbons (PAHs). It is a potential carcinogen and mutagen, known for its ability to induce cancer in laboratory animals. As an environmental pollutant, it can be released into the air, water, and soil through industrial processes and combustion of organic materials. 3,4-DIHYDROBENZ[A]ANTHRACEN-1(2H)-ONE has been the subject of research due to its potential health hazards and environmental impact.

57652-74-1

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57652-74-1 Usage

Uses

Used in Environmental Research:
3,4-Dihydrobenz[a]anthracen-1(2H)-one is used as a subject of study in environmental research for understanding its potential health hazards and environmental impact. Researchers investigate its presence in various ecosystems and its effects on human health and the environment.
Used in Toxicology Studies:
In toxicology studies, 3,4-dihydrobenz[a]anthracen-1(2H)-one is used as a test compound to evaluate its carcinogenic and mutagenic properties. This helps in understanding the mechanisms of its action and developing strategies to mitigate its harmful effects.
Used in Industrial Emission Control:
3,4-Dihydrobenz[a]anthracen-1(2H)-one is used as a target pollutant in industrial emission control strategies. Industries that release 3,4-DIHYDROBENZ[A]ANTHRACEN-1(2H)-ONE into the environment are required to implement measures to reduce its emission and minimize its impact on public health and the environment.
Used in Regulatory Frameworks:
3,4-Dihydrobenz[a]anthracen-1(2H)-one is used as a reference compound in regulatory frameworks to set limits and guidelines for its release into the environment. This helps in ensuring that industries adhere to safety standards and protect the environment from the harmful effects of 3,4-DIHYDROBENZ[A]ANTHRACEN-1(2H)-ONE.
Used in Public Health Education:
3,4-Dihydrobenz[a]anthracen-1(2H)-one is used as an example in public health education to raise awareness about the potential risks associated with exposure to environmental pollutants. This helps in promoting preventive measures and encouraging individuals to take steps to minimize their exposure to such harmful substances.

Check Digit Verification of cas no

The CAS Registry Mumber 57652-74-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,6,5 and 2 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 57652-74:
(7*5)+(6*7)+(5*6)+(4*5)+(3*2)+(2*7)+(1*4)=151
151 % 10 = 1
So 57652-74-1 is a valid CAS Registry Number.
InChI:InChI=1/C18H14O/c19-17-7-3-6-12-8-9-15-10-13-4-1-2-5-14(13)11-16(15)18(12)17/h1-2,4-5,8-11H,3,6-7H2

57652-74-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,4-dihydro-2H-benzo[a]anthracen-1-one

1.2 Other means of identification

Product number -
Other names EINECS 260-883-5

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:57652-74-1 SDS

57652-74-1Relevant academic research and scientific papers

Iron(II) and zinc(II) monohelical binaphthyl-salen complexes with overlapping benz[a]anthryl sidearms

Wiznycia, Alexander V.,Desper, John,Levy, Christopher J.

, p. 1520 - 1527 (2007/10/03)

The synthesis of the polyaromatic aldehyde 1-hydroxybenz[a]anthracene-2- carboxaldehyde is reported via a seven step protocol from 9,10- dihydroanthracene, with an overall yield of 30%. Two equivalents of the aldehyde are condensed with (R)-1,1′-binaphthyl-2,2′-diamine to produce a new binaphthyl-salen ligand, which is subsequently complexed to iron(ii) and zinc(ii) ions. The ligand and complexes are characterized by single-crystal X-ray crystallography. The complexes have distinct helical structures with overlapping benz[a]anthryl sidearms, and only M-helices are observed. The ligand and complexes are further characterized by solution 1H and 13C NMR spectroscopy as well as UV-visible and ECD spectroscopies. These studies indicate that there is a single component in solution, consistent with the solid state characterization. The Royal Society of Chemistry 2007.

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