CAS 19550-57-3
:6,7-DIMETHYL-1-TETRALONE
Description:
6,7-Dimethyl-1-tetralone is an organic compound characterized by its bicyclic structure, which consists of a naphthalene-like framework with a ketone functional group. It features two methyl groups attached to the 6 and 7 positions of the tetralone ring system, contributing to its unique chemical properties. The compound is typically a colorless to pale yellow liquid or solid, depending on its purity and temperature. It is known for its aromatic characteristics and can participate in various chemical reactions, including oxidation and reduction processes. 6,7-Dimethyl-1-tetralone is often utilized in organic synthesis and may serve as an intermediate in the production of pharmaceuticals, fragrances, and other fine chemicals. Its solubility in organic solvents makes it versatile for various applications in chemical research and industry. As with many organic compounds, safety precautions should be observed when handling it, as it may pose health risks if ingested or inhaled.
Formula:C12H14O
InChI:InChI=1/C12H14O/c1-8-6-10-4-3-5-12(13)11(10)7-9(8)2/h6-7H,3-5H2,1-2H3
SMILES:Cc1cc2CCCC(=O)c2cc1C
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Found 5 products.
6,7-Dimethyl-1-tetralone
CAS:Formula:C12H14OPurity:>98.0%(GC)Color and Shape:White to Almost white powder to crystalMolecular weight:174.246,7-Dimethyl-1-tetralone
CAS:Formula:C12H14OPurity:98.0%Color and Shape:SolidMolecular weight:174.23906,7-Dimethyl-1-tetralone
CAS:<p>Diels-Alder reactions are a type of reaction in organic chemistry that is used to form carbon-carbon bonds. The Diels-Alder reaction can be used to synthesize 6,7-dimethyl-1-tetralone. This compound is an example of a dienophile and can be used in the Diels-Alder reaction with a dienophile such as cyclopentadiene or norbornadiene. The equivalency of the diene and the dienophile is dependent on the relative stability of their corresponding enolate anion and cation.</p>Formula:C12H14OPurity:Min. 95%Molecular weight:174.24 g/mol





