CAS 2523-37-7
:9-Methylfluorene
Description:
9-Methylfluorene is an organic compound characterized by its structure, which consists of a fluorene backbone with a methyl group attached at the 9-position. This polycyclic aromatic hydrocarbon exhibits a fused ring system, contributing to its stability and unique electronic properties. It is typically a colorless to pale yellow solid at room temperature and is known for its relatively high melting and boiling points compared to simpler hydrocarbons. 9-Methylfluorene is soluble in organic solvents such as benzene and toluene but has limited solubility in water due to its hydrophobic nature. The compound is of interest in various fields, including organic electronics and materials science, due to its potential applications in light-emitting devices and as a building block for more complex organic molecules. Additionally, it can undergo typical aromatic reactions, such as electrophilic substitution, making it a versatile compound in synthetic organic chemistry. Safety data should be consulted, as with all chemical substances, to ensure proper handling and usage.
Formula:C14H12
InChI:InChI=1S/C14H12/c1-10-11-6-2-4-8-13(11)14-9-5-3-7-12(10)14/h2-10H,1H3
InChI key:InChIKey=ZVEJRZRAUYJYCO-UHFFFAOYSA-N
SMILES:CC1C=2C(C=3C1=CC=CC3)=CC=CC2
Synonyms:- 9-Methylfluorene
- 9H-Fluorene, 9-methyl-
- 9H-Fluorene, 9-methyl- (9CI)
- Ccris 4264
- Fluorene, 9-methyl-
- Nsc 10161
- 9-Methyl-9H-fluorene
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Found 6 products.
9-Methylfluorene
CAS:9-Methylfluorene is a polycyclic aromatic hydrocarbon (PAH) widely used in biochemical experiments and drug synthesis research.Formula:C14H12Molecular weight:180.259-Methylfluorene
CAS:Controlled ProductApplications 9-Methylfluorene has been shown to be mutagenic in Salmonella typhimurium TA98 and TA100 in the presence of 9000 X g supernantant from Aroclor-induced rats.
References Lavoie, E.J., et. al.: Mutat. Res., 91, 167 (1981)Formula:C14H12Color and Shape:NeatMolecular weight:180.25
