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7,14-diphenylacenaphtho[1,2-k]fluoranthene is a polycyclic aromatic hydrocarbon (PAH) chemical compound with a complex ring structure consisting of 20 carbon atoms. It is an environmental pollutant and a potential human carcinogen.
Used in Environmental Monitoring:
7,14-diphenylacenaphtho[1,2-k]fluoranthene is used as a biomarker for monitoring environmental pollution, particularly in areas with high levels of incomplete combustion such as industrial sites, coal tar production, and vehicle emissions.
Used in Public Health Research:
7,14-diphenylacenaphtho[1,2-k]fluoranthene is used as a subject of study in public health research to understand its potential adverse health effects, including respiratory issues and cancer, and to develop strategies for reducing exposure and mitigating its impact on human health.
Used in Industrial Processes:
7,14-diphenylacenaphtho[1,2-k]fluoranthene is produced as a byproduct in the burning of fossil fuels, the production of coke and aluminum, and other industrial processes. It is important to monitor and control its release into the environment to minimize its potential for bioaccumulation and adverse health effects.

7229-88-1

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7229-88-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7229-88-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,2 and 9 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7229-88:
(6*7)+(5*2)+(4*2)+(3*9)+(2*8)+(1*8)=111
111 % 10 = 1
So 7229-88-1 is a valid CAS Registry Number.

7229-88-1Downstream Products

7229-88-1Relevant academic research and scientific papers

Synthesis of fluoranthenes and indenocorannulenes: Elucidation of chiral stereoisomers on the basis of static molecular bowls

Wu, Yao-Ting,Hayama, Tomoharu,Baldridge, Kim K.,Linden, Anthony,Siegel, Jay S.

, p. 6870 - 6884 (2007/10/03)

Cycloaromatization of a peri diyne with an external alkyne provides a general route to indenofused polynuclear aromatics. Fluoranthenes 9 (or 13) are easily accessible in good to excellent yields (75-99%; 18 examples) from the reaction of symmetric (or as

Novel perylene chromophores obtained by a facile oxidative cyclodehydrogenation route

Wehmeier, Mike,Wagner, Manfred,Muellen, Klaus

, p. 2197 - 2205 (2007/10/03)

New perylene chromophores, phenyl-substituted diindeno[1,2,3-cd: 1′,2′,3′-lm]perylenes 5a,b and 4,4′,7,7′-tetraphenyldiacenaphtho[1,2- k:1′,2′,k′]diindeno[1,2,3-cd:1′,2′,3′- me]perylenes 22a,b, have been synthesized from substituted fluoranthene derivatives 3 a,b and 4 a,b by means of a surprisingly simple oxidative cyclodehydrogenation reaction. The resulting chromophores, when substituted with alkyl chains at the periphery, show good solubility in organic solvents, and a full characterization of the novel red, green, and blue dyes by field-desorption mass spectrometry, UV/Vis and 1H and 13C NMR spectroscopy becomes possible.

Polycyclic Aromatic Compounds: Part IX - A New Synthesis of Highly Arylated Fluoranthene Derivatives

Mondal, S.,Bandyopadhyay, T. K.,Bhattacharya, A. J.

, p. 225 - 229 (2007/10/02)

A new series of highly substituted fluoranthene derivatives (VIII), (XII) and (XIV) have been synthesised.The synthesis involves Diels-Alder cycloaddition of cyclopentadienones (I, II, III) to acenaphthylene.The carbonyl-bridged adducts (IV, IX) are cleav

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