2-Naphthalenemethanol, 6-methoxy- is an organic compound characterized by its naphthalene structure, which consists of two fused aromatic rings. The presence of a methanol group (-CH2OH) at the 2-position and a methoxy group (-OCH3) at the 6-position contributes to its chemical properties. This compound is typically a white to light yellow solid and is soluble in organic solvents, reflecting its aromatic nature. It may exhibit moderate polarity due to the hydroxyl and methoxy groups, which can participate in hydrogen bonding. The compound is of interest in various fields, including organic synthesis and medicinal chemistry, due to its potential biological activities. Its reactivity can be influenced by the functional groups present, allowing for various chemical transformations. Safety data should be consulted for handling and storage, as with any chemical substance, to ensure proper precautions are taken. Overall, 2-Naphthalenemethanol, 6-methoxy- is a versatile compound with applications in research and industry.

2-Naphthalenemethanol, 6-methoxy-

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(6-Methoxynaphthalen-2-yl)methanol is a fluorescent probe that reacts with cytosolic proteins. When (6-methoxynaphthalen-2-yl)methanol is incubated with human liver, the rate of reaction increases in proportion to the concentration of cytosolic proteins. This probe can be used to detect changes in the activity of dehydrogenase and aldehyde oxidase enzymes, which are responsible for the metabolism of alcohols and aldehydes. The fluorescence intensity also increases when (6-methoxynaphthalen-2-yl)methanol binds to proteins due to an increase in its chromophore.

CAS 60201-22-1: 2-Naphthalenemethanol, 6-methoxy-

(6-Methoxynaphthalen-2-yl)methanol

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(6-Methoxynaphthalen-2-Yl)Methanol

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6-Methoxy-2-naphthalenemethanol

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(6-Methoxynaphthalen-2-yl)Methanol

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(6-Methoxynaphthalen-2-yl)methanol

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