Date published: 2025-10-5

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1-Methylfluorene (CAS 1730-37-6)

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CAS Number:
1730-37-6
Molecular Weight:
180.25
Molecular Formula:
C14H12
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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1-Methylfluorene (1-MF) derived from fluorene, a naturally occurring hydrocarbon found in coal tar, serves as an essential building block for synthesizing various compounds. Notably, it serves as a precursor in the production of fluorenone, a key component in the manufacturing of polymers and other materials. The significance of 1-Methylfluorene extends beyond its role as a precursor, as it also finds use as a reagent in organic synthesis. Its participation in chemical reactions facilitates the creation of intricate molecular structures. Moreover, its properties as a fluorescent dye make it an invaluable tool for imaging and tracking biological processes, providing insights into complex biological phenomena. 1-Methylfluorene additionally serves as a model compound in studying the structure and reactivity of aromatic hydrocarbons. By examining its properties and behavior, researchers gain valuable insights applicable to a wide range of aromatic hydrocarbon compounds. With its distinctive planar structure characterized by alternating double and single bonds, 1-Methylfluorene demonstrates the ability to interact with other molecules through various means, including van der Waals interactions, hydrogen bonds, and pi-pi stacking.


1-Methylfluorene (CAS 1730-37-6) References

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  2. Transformation of Substituted Fluorenes and Fluorene Analogs by Pseudomonas sp. Strain F274.  |  Grifoll, M., et al. 1995. Appl Environ Microbiol. 61: 3490-3. PMID: 16535132
  3. Biodegradation kinetics of select polycyclic aromatic hydrocarbon (PAH) mixtures by Sphingomonas paucimobilis EPA505.  |  Desai, AM., et al. 2008. Biodegradation. 19: 223-33. PMID: 17534722
  4. Structure-related clustering of gene expression fingerprints of thp-1 cells exposed to smaller polycyclic aromatic hydrocarbons.  |  Wan, B., et al. 2008. SAR QSAR Environ Res. 19: 351-73. PMID: 18637284
  5. Methylated derivatives of pyrene and fluorene: evaluation of genotoxicity in the hepatocyte/DNA repair test and tumorigenic activity in newborn mice.  |  Rice, JE., et al. 1987. J Toxicol Environ Health. 21: 525-32. PMID: 3599094
  6. Bay or baylike regions of polycyclic aromatic hydrocarbons were potent inhibitors of Gap junctional intercellular communication.  |  Weis, LM., et al. 1998. Environ Health Perspect. 106: 17-22. PMID: 9417772
  7. Vibrational spectra of fluorene, 1-methylfluorene and 1,8-dimethylfluorene  |  Shubhadip Chakraborty a, Prasanta Das a, Sadasivam Manogaran b, Puspendu K. Das a. 2013. Vibrational Spectroscopy. 68: 162-169.
  8. Biodegradation of PAHs by Ligninolytic Fungi Hypoxylon Fragiforme and Coniophora Puteana  |  Mustafa Memić, Margareta Vrtačnik, Bojana Boh, Franc Pohleven & Omer Mahmutović. 2017. Polycyclic Aromatic Compounds. 40: 206-213.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

1-Methylfluorene, 250 mg

sc-229800
250 mg
$235.00