CAS 6682-69-5
:1H-Inden-1-one, 2,3-dihydro-5,7-dimethyl-
Description:
1H-Inden-1-one, 2,3-dihydro-5,7-dimethyl- is an organic compound characterized by its bicyclic structure, which includes an indene core with a ketone functional group. This compound features two methyl groups at the 5 and 7 positions of the indene ring, contributing to its unique chemical properties and potential reactivity. It is typically a colorless to pale yellow liquid or solid, depending on its purity and specific conditions. The presence of the ketone group suggests that it may participate in various chemical reactions, such as nucleophilic additions or condensation reactions. Additionally, its structure allows for potential applications in organic synthesis, pharmaceuticals, and materials science. The compound's CAS number, 6682-69-5, is a unique identifier that facilitates its identification in chemical databases and literature. As with many organic compounds, its physical and chemical properties, such as solubility, boiling point, and stability, can vary based on environmental conditions and the presence of other substances.
Formula:C11H12O
Synonyms:- 5,7-Dimethyl-1-indanone
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Found 4 products.
5,7-Dimethyl-2,3-dihydroinden-1-one
CAS:<p>5,7-Dimethyl-2,3-dihydroinden-1-one</p>Purity:98%Molecular weight:160.21g/mol5,7-Dimethyl-2,3-dihydro-1H-inden-1-one
CAS:<p>5,7-Dimethyl-2,3-dihydro-1H-inden-1-one is a cytotoxic agent that is used in vivo to study tumor models. It has been shown to be potent and cytotoxic against tumor cells. The drug inhibits the growth of colon cancer cells by binding to the DNA chain at the level of purine nucleoside phosphorylase. 5,7-Dimethyl-2,3-dihydro-1H-inden-1-one also inhibits carboxamides and lipophilic substituents in the cell membrane. This drug is also an inhibitor that blocks purine nucleoside phosphorylase and prevents synthesis of purines from ATP and hypoxanthine.</p>Formula:C11H12OPurity:Min. 95%Molecular weight:160.21 g/mol
