CAS 442-66-0
:1,7-dimethyl-9H-fluorene
Description:
1,7-Dimethyl-9H-fluorene, with the CAS number 442-66-0, is an organic compound belonging to the class of polycyclic aromatic hydrocarbons (PAHs). It features a fluorene backbone, which consists of a fused ring system comprising a phenyl group and a cyclopentane ring. The presence of two methyl groups at the 1 and 7 positions of the fluorene structure contributes to its unique chemical properties. This compound is typically characterized by its solid state at room temperature, exhibiting a white to pale yellow crystalline appearance. It is relatively insoluble in water but soluble in organic solvents such as benzene and toluene. 1,7-Dimethyl-9H-fluorene is of interest in various fields, including materials science and organic electronics, due to its potential applications in the development of organic semiconductors and light-emitting devices. Additionally, like other PAHs, it may pose environmental and health concerns, necessitating careful handling and assessment of its toxicity and environmental impact.
Formula:C15H14
InChI:InChI=1/C15H14/c1-10-6-7-13-12(8-10)9-15-11(2)4-3-5-14(13)15/h3-8H,9H2,1-2H3
SMILES:Cc1ccc2c(c1)Cc1c(C)cccc21
Synonyms:- 9H-fluorene, 1,7-dimethyl-
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1,7-Dimethylfluorene
CAS:<p>Applications 1,7-Dimethylfluorene is a product of the selenium dehydrogenation of gibberic acid. 1,7-Dimethylfluorene is also one of the many polyaromatic hydrocarbons (PAH) that are found within lake sediments, negatively impacting zoo plankton changes in the water, as well as the ecosystems that reside there.<br>References Dimond, A.: Prog. Ch. Org. Nat. Prod., 17, 298 (1959); Kurek, J., et al.: P. Natl. Acad. Sci. USA, 110, 1761 (2013); Mulholland, T. & Ward, G.: J. Chem. Soc., No vol. no. given, 4676 (1954);<br></p>Formula:C15H14Color and Shape:NeatMolecular weight:194.27
