CAS 13621-25-5
:3,4-Dihydro-5,7-dimethyl-1(2H)-naphthalenone
Description:
3,4-Dihydro-5,7-dimethyl-1(2H)-naphthalenone, with the CAS number 13621-25-5, is an organic compound belonging to the naphthalenone class. This substance features a naphthalene ring system that is partially saturated, indicating the presence of a double bond in the structure. The compound is characterized by the presence of two methyl groups at the 5 and 7 positions, which contribute to its hydrophobic nature and influence its chemical reactivity. The ketone functional group at the 1-position is responsible for its reactivity and potential applications in organic synthesis. Typically, compounds of this type exhibit moderate to low solubility in water but are more soluble in organic solvents. They may also display interesting biological activities, making them of interest in medicinal chemistry. The structural features of 3,4-Dihydro-5,7-dimethyl-1(2H)-naphthalenone suggest potential uses in various chemical applications, including as intermediates in the synthesis of more complex molecules.
Formula:C12H14O
InChI:InChI=1S/C12H14O/c1-8-6-9(2)10-4-3-5-12(13)11(10)7-8/h6-7H,3-5H2,1-2H3
InChI key:InChIKey=UYJCNOMEGPDXMV-UHFFFAOYSA-N
SMILES:CC1=C2C(=CC(C)=C1)C(=O)CCC2
Synonyms:- 1(2H)-Naphthalenone, 3,4-dihydro-5,7-dimethyl-
- 3,4-Dihydro-5,7-dimethyl-1(2H)-naphthalenone
- 3,4-Dihydro-5,7-dimethylnaphthalen-1(2H)-one
- 5,7-Dimethyl-1,2,3,4-tetrahydro-1-naphthalenone
- 5,7-Dimethyl-3,4-dihydro-2H-naphthalen-1-one
- 5,7-dimethyl-3,4-dihydronaphthalen-1(2H)-one
- NSC 63113
- 5,7-Dimethyl-1-tetralone
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Found 4 products.
3,4-Dihydro-5,7-dimethylnaphthalen-1(2H)-one
CAS:3,4-Dihydro-5,7-dimethylnaphthalen-1(2H)-onePurity:≥95%Color and Shape:SolidMolecular weight:174.24g/mol5,7-Dimethyl-1-tetralone
CAS:<p>5,7-Dimethyl-1-tetralone is a coumarin derivative that is a single-crystal x-ray analysis preparative. It has been found to undergo cross-coupling reaction with a variety of organometallic reagents. 5,7-Dimethyl-1-tetralone can be used as a research chemical in the synthesis of other chemicals and pharmaceuticals. Cross coupling reactions with lithium diisopropylamide have been shown to produce 6-methoxy-1-tetralone which can be saponified to form an intermediate for the synthesis of drugs. The tautomerization process is also mediated by the solvent and the reaction time.</p>Formula:C12H14OPurity:Min. 95%Molecular weight:174.24 g/mol



