5-Nitro-3,4-dihydronaphthalen-1(2H)-one, with the CAS number 51114-73-9, is an organic compound characterized by its naphthalene structure, which is a bicyclic aromatic hydrocarbon. This compound features a nitro group (-NO2) and a ketone functional group (C=O) attached to the naphthalene ring system. The presence of the nitro group introduces polar characteristics, which can influence its solubility and reactivity. Typically, compounds like this may exhibit moderate to low solubility in water but can be more soluble in organic solvents. The dihydronaphthalene structure suggests that it has two hydrogen atoms added to the naphthalene framework, which can affect its stability and reactivity. This compound may be of interest in various chemical syntheses, particularly in the development of pharmaceuticals or agrochemicals, due to the reactivity of both the nitro and ketone groups. Additionally, its unique structure may impart specific biological activities, making it a candidate for further research in medicinal chemistry.

5-nitro-3,4-dihydronaphthalen-1(2H)-one

51114-73-9: 5-Nitro-3,4-dihydronaphthalen-1(2H)-one, with the CAS number 51114-73-9, is an organic compound characterized by its naphthalene structure, which is a bicyclic aromatic hydrocarbon. This compound features a nitro group (-NO2) and a ketone functional group (C=O) attached to the naphthalene ring system. The presence of the nitro group introduces polar characteristics, which can influence its solubility and reactivity. Typically, compounds like this may exhibit moderate to low solubility in water but can be more soluble in organic solvents. The dihydronaphthalene structure suggests that it has two hydrogen atoms added to the naphthalene framework, which can affect its stability and reactivity. This compound may be of interest in various chemical syntheses, particularly in the development of pharmaceuticals or agrochemicals, due to the reactivity of both the nitro and ketone groups. Additionally, its unique structure may impart specific biological activities, making it a candidate for further research in medicinal chemistry.

CAS 51114-73-9

5-nitro-3,4-dihydronaphthalen-1(2H)-one

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