5-Nitro-1,3-dihydroisobenzofuran is an organic compound characterized by its unique bicyclic structure, which includes a furan ring fused to a benzene-like system. The presence of a nitro group at the 5-position contributes to its reactivity and potential applications in organic synthesis. This compound typically exhibits a pale yellow to brownish color and is soluble in organic solvents, reflecting its non-polar characteristics. Its molecular structure suggests that it may participate in various chemical reactions, including electrophilic substitutions due to the electron-withdrawing nature of the nitro group. Additionally, the dihydroisobenzofuran framework can influence its physical properties, such as boiling and melting points, as well as its stability under different conditions. As with many nitro compounds, it may pose certain hazards, including potential toxicity and environmental concerns, necessitating careful handling and disposal. Overall, 5-Nitro-1,3-dihydroisobenzofuran serves as an interesting compound for research in synthetic organic chemistry and materials science.

5-Nitro-1,3-dihydroisobenzofuran

52771-99-0: 5-Nitrophthalan, 5-Nitro-1,3-Dihydro-2-Benzofuran

1,3-Dihydro-5-nitro-isobenzofuran is a chemical compound that is used as a probe for metal cations in biological samples. 1,3-Dihydro-5-nitro-isobenzofuran has been shown to be activated by hydroxide and p-hydroxybenzoic acid, which generate the corresponding nitrite anion and the corresponding hydroxybenzoate anion. This reaction is catalyzed by aerobacter aerogenes. The nitrite anion can be detected with probes labeled with colorants such as phenol red or 2,4-dinitrophenylhydrazine. In this way, 1,3-dihydro-5-nitroisobenzofuran can be used to detect the presence of iron ions in biological samples such as blood or urine.

CAS 52771-99-0: 5-Nitro-1,3-dihydroisobenzofuran

5-Nitro-1,3-dihydroisobenzofuran

Ref: IN-DA00DB1K

1,3-Dihydro-5-nitro-isobenzofuran

Ref: 3D-FD150751

5-NITRO-1,3-DIHYDROISOBENZOFURAN

Ref: 10-F469000