5385-22-8 Usage
Description
NAPHTHO[1,2-B]FLUORANTHENE is a complex organic compound belonging to the family of polycyclic aromatic hydrocarbons (PAHs). It is characterized by its large, planar structure composed of multiple fused benzene rings. Due to its unique chemical and physical properties, NAPHTHO[1,2-B]FLUORANTHENE has potential applications in various fields.
Uses
Used in Chemical Research:
NAPHTHO[1,2-B]FLUORANTHENE is used as a research compound for studying the properties and behavior of PAHs. Its unique structure allows scientists to investigate the effects of molecular geometry on chemical reactivity, stability, and interactions with other molecules.
Used in Material Science:
In the field of material science, NAPHTHO[1,2-B]FLUORANTHENE can be used as a component in the development of advanced materials with specific optical, electronic, or structural properties. Its planar structure and conjugated system make it a promising candidate for applications in organic electronics, such as organic light-emitting diodes (OLEDs) or organic photovoltaics (OPVs).
Used in Environmental Monitoring:
Due to its structural similarity to other PAHs, NAPHTHO[1,2-B]FLUORANTHENE can be used as a reference compound in environmental monitoring and assessment of PAH contamination. Understanding the distribution, transport, and fate of this compound in the environment can provide insights into the behavior of other, potentially more hazardous PAHs.
Check Digit Verification of cas no
The CAS Registry Mumber 5385-22-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,8 and 5 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5385-22:
(6*5)+(5*3)+(4*8)+(3*5)+(2*2)+(1*2)=98
98 % 10 = 8
So 5385-22-8 is a valid CAS Registry Number.
5385-22-8Relevant articles and documents
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Lavit-Lamy,D.,Buu-Hoi,N.P.
, p. 92 - 94 (1966)
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Acephenanthrylenes from flash vacuum thermolysis of diarylmethylidenecycloproparenes
Halton, Brian
, p. 1077 - 1079 (2007/10/03)
Upon flash vacuum thermolysis at 750°C fluorenylidenecyclopropa[b] naphthalene (1) undergoes opening of the three-membered ring and rearrangement to give a range of C24H14 polycyclic aromatic hydrocarbons. Dibenz[e.l]- and -[e.k]acephenanthrylene (7) and (12), respectively, have been identified while the plausible naphth[1,2-e]- and [2,3-e]acephenanthrylenes (9) and (14) were not detected. With diphenylmethylidenecyclopropa[b]naphthalene (2) cyclodehydrogenation and rearrangement also provide C24H14 polycycles; dibenz[e.k]acephenanthrylene (12) is identified and dibenz[a.e]aceanthrylene (15) is a proposed product.
