From WikiMD's Food, Medicine & Wellness Encyclopedia


1,1,6-Trimethyl-1,2-dihydronaphthalene is an organic compound with the chemical formula C_13H_16. It is a derivative of naphthalene, a bicyclic aromatic hydrocarbon, where two of the carbon atoms in the naphthalene structure are saturated, and the molecule is further substituted with three methyl groups. This compound belongs to the class of chemical compounds known as dihydronaphthalenes, which are characterized by having a naphthalene skeleton partially saturated.

Structure and Properties[edit | edit source]

1,1,6-Trimethyl-1,2-dihydronaphthalene features a unique structure due to its partial saturation and methyl substitutions. The saturation occurs at the 1 and 2 positions of the naphthalene ring, making it a dihydronaphthalene. The methyl groups at positions 1 and 6 add to the complexity of its chemical behavior and physical properties. This compound is a clear example of how slight modifications in the structure of a hydrocarbon can significantly alter its chemical and physical properties.

Synthesis[edit | edit source]

The synthesis of 1,1,6-Trimethyl-1,2-dihydronaphthalene typically involves the hydrogenation of naphthalene derivatives that are already substituted with methyl groups. This process requires specific conditions, including the presence of a catalyst such as palladium on carbon (Pd/C) and an appropriate hydrogen source, under controlled temperature and pressure. The exact synthetic route can vary depending on the starting materials and the desired specificity of the substitution pattern on the naphthalene ring.

Applications[edit | edit source]

While specific applications of 1,1,6-Trimethyl-1,2-dihydronaphthalene may not be widely documented, compounds of this nature often find utility in the synthesis of other complex organic molecules. They can serve as intermediates in the production of pharmaceuticals, agrochemicals, and dyes. Their unique structural features make them valuable in studying the relationship between the structure of hydrocarbon compounds and their reactivity, stability, and physical properties.

Safety and Environmental Impact[edit | edit source]

As with many organic compounds, the safety and environmental impact of 1,1,6-Trimethyl-1,2-dihydronaphthalene depend on its concentration and the context of its use. Proper handling, storage, and disposal guidelines should be followed to minimize any potential health risks and environmental contamination. The compound's effects on human health and the environment have not been extensively studied, indicating the need for careful consideration in its use and disposal.


Navigation: Wellness - Encyclopedia - Health topics - Disease Index‏‎ - Drugs - World Directory - Gray's Anatomy - Keto diet - Recipes

Search WikiMD

Ad.Tired of being Overweight? Try W8MD's physician weight loss program.
Semaglutide (Ozempic / Wegovy and Tirzepatide (Mounjaro / Zepbound) available.
Advertise on WikiMD

WikiMD is not a substitute for professional medical advice. See full disclaimer.

Credits:Most images are courtesy of Wikimedia commons, and templates Wikipedia, licensed under CC BY SA or similar.

Contributors: Prab R. Tumpati, MD