CAS 79795-25-8
:5-methoxy-2-methylnaphthalen-1-ol
Description:
5-Methoxy-2-methylnaphthalen-1-ol, with the CAS number 79795-25-8, is an organic compound belonging to the naphthalene family, characterized by a naphthalene backbone substituted with a methoxy group and a hydroxyl group. This compound typically appears as a solid or viscous liquid, depending on its purity and temperature. It is known for its aromatic properties, which can contribute to its potential applications in fragrance and flavor industries. The presence of the hydroxyl group indicates that it can participate in hydrogen bonding, influencing its solubility in polar solvents. Additionally, the methoxy group can affect the compound's reactivity and stability, making it of interest in various chemical syntheses. Its structural features may also impart biological activity, warranting investigation in pharmacological contexts. Overall, 5-methoxy-2-methylnaphthalen-1-ol is a compound of interest in both synthetic organic chemistry and potential applications in medicinal chemistry.
Formula:C12H12O2
InChI:InChI=1/C12H12O2/c1-8-6-7-9-10(12(8)13)4-3-5-11(9)14-2/h3-7,13H,1-2H3
SMILES:Cc1ccc2c(cccc2OC)c1O
Synonyms:- 1-Naphthalenol, 5-methoxy-2-methyl-
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Found 1 products.
5-Methoxy-2-methyl-Alpha-naphthol-d3
CAS:Controlled ProductApplications 5-Methoxy-2-methyl-α-naphthol-d3 is an intermediate in the synthesis of Plumbagin-d3 (P627002). Plumbagin-d3 is labelled Plumbagin (P627000) which induces apoptosis in cancer cells. It also inhibits NADPH oxidase 4 in a time- and dose-dependent manner.
References Klotz, L., et al.: Molecules, 19 14902 (2014); Gupta, S., et al.: Cancer Metastasis Rev., 29, 405 (2010); Schramm, A., et al.: Vascul. Pharmacol., 56, 216 (2012)Formula:C12H9D3O2Color and Shape:NeatMolecular weight:191.24
