2,3-Dihydro-1H-indene-1,2-diol, with the CAS number 4370-02-9, is an organic compound characterized by its bicyclic structure, which includes a fused indene ring system. This compound features two hydroxyl (-OH) groups located at the 1 and 2 positions of the indene framework, contributing to its reactivity and potential applications in organic synthesis. It is typically a colorless to pale yellow liquid or solid, depending on its purity and form. The presence of hydroxyl groups makes it a potential candidate for hydrogen bonding, influencing its solubility in polar solvents like water and alcohols. Additionally, 2,3-dihydro-1H-indene-1,2-diol may exhibit antioxidant properties and could be utilized in various chemical reactions, including those involving nucleophilic substitutions or as intermediates in the synthesis of more complex organic molecules. Its unique structure and functional groups make it of interest in fields such as medicinal chemistry and materials science.

2,3-dihydro-1H-indene-1,2-diol

4370-02-9: 1H-indene-1,2-diol, 2,3-dihydro-, Indane-1,2-diol

1,2-Dihydroxyindan is a synthetic solid catalyst that has been shown to be an effective inhibitor of the fungal strain Penicillium. It can be used in the synthesis of acetate extract, which is an important intermediate in the production of antibiotics. 1,2-Dihydroxyindan has been shown to inhibit human immunodeficiency virus (HIV) strains by binding to the substrate binding site. This agent also inhibits lipase activity and isomers of alicyclic compounds.

CAS 4370-02-9: 2,3-dihydro-1H-indene-1,2-diol

1,2-Dihydroxyindan

Ref: 3D-EAA37002

1,2-Dihydroxyindan

Ref: 3B-D3311

1,2-DIHYDROXYINDANE

Ref: IN-DA003DEG

1,2-Dihydroxyindane

Ref: 54-OR937916