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Fluoreno<3,2,1,9-defg>chrysene is a polycyclic aromatic hydrocarbon (PAH) consisting of five fused benzene rings, with a molecular formula of C22H12. It is a structural isomer of chrysene, characterized by the presence of a fluorene moiety fused to the chrysene core. fluoreno<3,2,1,9-defg>chrysene is known for its potential environmental and health impacts, as PAHs are often found in polluted air, water, and soil, and can be carcinogenic. Fluoreno<3,2,1,9-defg>chrysene is formed during the incomplete combustion of organic materials, such as coal, oil, and gas, and is also present in tobacco smoke. Due to its complex structure and potential toxicity, it is a subject of interest in environmental chemistry and toxicology research.

192-35-8

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192-35-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 192-35-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,9 and 2 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 192-35:
(5*1)+(4*9)+(3*2)+(2*3)+(1*5)=58
58 % 10 = 8
So 192-35-8 is a valid CAS Registry Number.

192-35-8Downstream Products

192-35-8Relevant academic research and scientific papers

SYNTHESIS OF POLYCYCLIC AROMATIC FLUORANTHENES

Cho, Bongsup P.,Harvey, Ronald G.

, p. 861 - 864 (2007/10/02)

A general synthetic approach to polycyclic aromatic hydrocarbons containing a fluoranthene ring system is described.The method entails fusion of an indeno ring to an alternant hydrocarbon via reaction of an aryllithium derivative with cyclohexene oxide.

Policyclic Fluoranthene Hydrocarbons. 2. A New General Synthesis

Cho, Bongsup P.,Harvey, Ronald G.

, p. 5668 - 5678 (2007/10/02)

A novel and efficient synthetic approach to policyclic fluoranthene hydrocarbons is described.The method entails fusion of an indeno ring to an appropriate alternant hydrocarbon via reaction of its aryllithium derivative with cyclohexene oxide, followed by oxidation, cyclodehydration, and aromatization.Cyclization of the cyclohexanone and cyclohexanol derivatives of the policyclic aromatic ring systems studied proceeds with high regioselectivity, and the direction of ring closure is predictable by molecular orbital methods.This synthetic approach provides a convenient general route to polyaromatic fluoranthene compounds, including potentially carcinogenic members of this class.Hydrocarbons synthesized by this method include benzacephenanthrylene (1), indenopyrene (2), indenochrysene (3), benzindenochrysene (4), fluorenochrysene (5), dibenzaceanthrylene (6), dibenzaceanthrylene (7), benzaceanthrylene (8), benzindenochrysene (9), fluorenochrysene (10), and dibenzacephenanthrylene (11).

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