CAS 30364-38-6
:1,1,6-Trimethyl-1,2-dihydronaphthalene
Description:
1,1,6-Trimethyl-1,2-dihydronaphthalene is an organic compound belonging to the class of polycyclic aromatic hydrocarbons. It features a naphthalene backbone with three methyl groups attached at the 1, 1, and 6 positions, contributing to its unique structural characteristics. This compound is typically colorless to pale yellow in appearance and is known for its aromatic odor. It is relatively hydrophobic, indicating low solubility in water but higher solubility in organic solvents. The presence of multiple methyl groups enhances its stability and influences its physical properties, such as boiling and melting points. 1,1,6-Trimethyl-1,2-dihydronaphthalene is often utilized in the fragrance industry due to its pleasant scent and is also studied for its potential applications in materials science and organic synthesis. As with many aromatic compounds, it is important to handle it with care, considering potential health and environmental impacts. Safety data sheets should be consulted for specific handling and storage guidelines.
Formula:C13H16
InChI:InChI=1S/C13H16/c1-10-6-7-12-11(9-10)5-4-8-13(12,2)3/h4-7,9H,8H2,1-3H3
InChI key:InChIKey=RTUMCNDCAVLXEP-UHFFFAOYSA-N
SMILES:CC1(C)C=2C(=CC(C)=CC2)C=CC1
Synonyms:- 1,1,6-Trimethyl-1,2-dihydronaphthalene
- 1,1,6-Trimethyl-2H-naphthalene
- Dehydro-ar-ionene
- Naphthalene, 1,2-dihydro-1,1,6-trimethyl-
- 1,2-Dihydro-1,1,6-trimethylnaphthalene
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Found 2 products.
Naphthalene, 1,2-dihydro-1,1,6-trimethyl-
CAS:Formula:C13H16Color and Shape:LiquidMolecular weight:172.26611,2-Dihydro-1,1,6-trimethylnaphthalene (>80%)
CAS:Controlled Product<p>Applications 1,2-Dihydro-1,1,6-trimethyl-naphthalene is responsible for a "kerosene note" or "petrol" aromas in aged Riesling wines.<br>References Sacks, G., et al.: J. Agri. Food Chem., 60, 2998 (2012); Winterhalter, P., et al.: ACS Symposium Series, 1134, 125 (2013)<br></p>Formula:C13H16Purity:>80%Color and Shape:Colourless OilyMolecular weight:172.27

