Molecular structure of 3-Methyl-1-indanone, CAS Number: 6072-57-7
3-Methyl-1-indanone (CAS 6072-57-7)
CAS Number:
6072-57-7
Molecular Weight:
146.19
Molecular Formula:
C10H10O
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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3-Methyl-1-indanone is an organic compound classified as a ketone. It presents itself as a colorless liquid with a relatively low boiling point. While the precise mechanism of action of 3-Methyl-1-indanone remains incompletely understood, it is recognized that the compound interacts with specific proteins and enzymes. Additionally, it has the capability to interact with DNA. Furthermore, 3-Methyl-1-indanone has been observed to influence gene expression and impact the activity of certain enzymes.
3-Methyl-1-indanone (CAS 6072-57-7) References
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- Unresolved complex mixtures (UCMs) of aromatic hydrocarbons: branched alkyl indanes and branched alkyl tetralins are present in UCMs and accumulated by and toxic to, the mussel Mytilus edulis. | Booth, AM., et al. 2008. Environ Sci Technol. 42: 8122-6. PMID: 19031912
- Synthesis of chiral 3-alkyl-3,4-dihydroisocoumarins by dynamic kinetic resolutions catalyzed by a Baeyer-Villiger monooxygenase. | Rioz-Martínez, A., et al. 2010. J Org Chem. 75: 2073-6. PMID: 20166716
- Stereocontrolled synthesis of substituted chiral piperidines via one-pot asymmetric 6π-azaelectrocyclization: asymmetric syntheses of (-)-dendroprimine, (+)-7-epidendroprimine, (+)-5-epidendroprimine, and (+)-5,7-epidendroprimine. | Kobayashi, T., et al. 2012. J Org Chem. 77: 1812-32. PMID: 22263723
- Photoinduced intramolecular cyclopentanation vs photoprotolytic oxametathesis in polycyclic alkenes outfitted with conformationally constrained aroylmethyl chromophores. | Valiulin, RA., et al. 2013. J Org Chem. 78: 2012-25. PMID: 23106813
- Structure-activity relationship of indoloquinoline analogs anti-MRSA. | Zhao, M., et al. 2015. Bioorg Med Chem Lett. 25: 5551-4. PMID: 26522949
- Current Status on the Functional Characterization of Chemosensory Receptors of Cydia pomonella (Lepidoptera: Tortricidae). | Cattaneo, AM. 2018. Front Behav Neurosci. 12: 189. PMID: 30210318
- Two-Carbon Ring Expansion of 1-Indanones via Insertion of Ethylene into Carbon-Carbon Bonds. | Xia, Y., et al. 2019. J Am Chem Soc. 141: 13038-13042. PMID: 31389237
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| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
3-Methyl-1-indanone, 1 g | sc-231821 | 1 g | $55.00 |