6-Nitro-2-tetralone is an organic compound characterized by its nitro and ketone functional groups. It belongs to the class of tetralones, which are bicyclic compounds featuring a fused benzene and cyclopentane ring structure. The presence of the nitro group at the 6-position of the tetralone structure contributes to its reactivity and potential applications in organic synthesis. This compound typically appears as a solid and is known for its relatively low solubility in water, while being more soluble in organic solvents. Its molecular structure allows for various chemical transformations, making it a valuable intermediate in the synthesis of pharmaceuticals and agrochemicals. Additionally, the nitro group can participate in electrophilic aromatic substitution reactions, enhancing its utility in synthetic chemistry. As with many nitro compounds, safety precautions should be taken due to potential toxicity and environmental concerns. Overall, 6-Nitro-2-tetralone is a significant compound in the field of organic chemistry, with diverse applications stemming from its unique structural features.

6-Nitro-2-tetralone

200864-16-0: 6-Nitro-3,4-dihydro-1H-naphthalen-2-one, 6-nitro-3,4-dihydronaphthalen-2(1H)-one

6-Nitro-3,4-dihydro-1H-naphthalen-2-one is an anion that has a carbonyl group with the hydroxide ion acting as the conjugate base. The deprotonation of the enolate leads to an equilibrium between the enolate and the protonated form. The transfer of a proton from one molecule to another will cause an imbalance in the concentration of these species. This reaction can be observed by spectroscopy, and is best studied using NMR spectroscopy. The kinetic constants for this reaction are determined by measuring the rate at which it takes place at various temperatures, while thermodynamic constants are obtained by measuring enthalpy changes during the reaction.

CAS 200864-16-0: 6-Nitro-2-tetralone

6-Nitro-3,4-dihydro-1H-naphthalen-2-one

Ref: 3D-FN151239

2(1H)-Naphthalenone, 3,4-dihydro-6-nitro-

Ref: IN-DA002D1B