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12-(naphthaleN-2yl)benoza[a]athracene, also known as Benzo[a]pyrene (B[a]P), is a polycyclic aromatic hydrocarbon (PAH) and a potent environmental pollutant. It is commonly found in sources such as cigarette smoke, automobile exhaust, and grilled food. B[a]P is recognized as a human carcinogen and is classified as a Group 1 carcinogen by the International Agency for Research on Cancer (IARC). 12-(naphthaleN-2yl)benoza[a]athracene is notorious for its ability to cause mutations and the development of cancer through the formation of reactive intermediates that bind to cellular DNA.

116027-92-0

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116027-92-0 Usage

Uses

Used in Environmental and Health Research:
12-(naphthaleN-2yl)benoza[a]athracene is used as a subject of study in environmental and health research to understand its impact on human health and the environment. The research aims to investigate the mechanisms of its carcinogenic properties, its presence in various environmental compartments, and ways to mitigate its harmful effects.
Used in Toxicology Studies:
In toxicology, 12-(naphthaleN-2yl)benoza[a]athracene is used as a model compound to study the effects of exposure to environmental pollutants. It helps researchers to understand the dose-response relationships and the potential for adverse health effects, including cancer and reproductive and developmental toxicity.
Used in Analytical Chemistry:
12-(naphthaleN-2yl)benoza[a]athracene is utilized in analytical chemistry for the development and validation of methods to detect and quantify PAHs in environmental and biological samples. Accurate measurement of B[a]P levels is crucial for assessing exposure risks and implementing regulatory controls.
Used in Public Health Policy and Regulation:
Information gathered from studies on 12-(naphthaleN-2yl)benoza[a]athracene is used to inform public health policy and regulation. It aids in the establishment of safety standards and guidelines to reduce human exposure to this potent carcinogen, thereby protecting public health.
Used in Environmental Remediation:
12-(naphthaleN-2yl)benoza[a]athracene is a target compound in environmental remediation efforts. Technologies and strategies are developed to remove or degrade B[a]P from contaminated sites, such as soil and water bodies, to mitigate its impact on ecosystems and human health.

Check Digit Verification of cas no

The CAS Registry Mumber 116027-92-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,0,2 and 7 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 116027-92:
(8*1)+(7*1)+(6*6)+(5*0)+(4*2)+(3*7)+(2*9)+(1*2)=100
100 % 10 = 0
So 116027-92-0 is a valid CAS Registry Number.

116027-92-0Downstream Products

116027-92-0Relevant academic research and scientific papers

ORGANIC LIGHT DEVICE AND ORGANIC LIGHT COMPOUND FOR THE SAME

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, (2016/10/09)

PURPOSE: An organic photoelectric element is provided to obtain high luminous efficiency, luminance, color purity, and remarkably improved luminous life time. CONSTITUTION: An organic photoelectric element comprises a first electrode, a second electrode, and at least one organic layer between the first electrode, and the second electrode, the organic film comprises an organic luminous compound in chemical formula L. In chemical formula L, R1 and R2 are different each other, and is respectively selected from hydrogen, deuterium, C1-40 alkyl, C2-40 alkenyl, C2-40 alkynyl, C5-40 aryl, C5-40 heteroaryl, C5-40 aryloxy, C1-40 alkyloxy, C5-40 arylamino, C5-40 diarylamino, C6-40 arylalkyl, C3-40 cycloalkyl and C3-40 heterocycloalkyl, or is a group forming a fused aliphatic ring, a condensed aromatic ring, a condensed hetero aliphatic ring, or a condensed hetero aromatic ring with a neighboring group.

Improved synthesis of aryl-substituted anthracenes and heteroacenes

Li, Guijie,Zhou, Shaolin,Su, Guowei,Liu, Yuanhong,Wang, Peng George

, p. 9830 - 9833 (2008/03/28)

(Chemical Equation Presented) A Bronsted acid-catalyzed highly efficient construction of substituted arylanthracenes and heteroacenes is described, which is assumed to be initiated through the facile formation of a benzylic cation intermediate. This method offers several advantages in comparison with known aromatic cyclodehydration reactions such as high selectivities, mild reaction conditions, and easily accessible starting materials.

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