5-Aminoindan-1-one is an organic compound characterized by its indanone structure, which features a fused benzene and cyclopentane ring system. The presence of an amino group (-NH2) at the 5-position of the indanone contributes to its reactivity and potential biological activity. This compound typically appears as a solid at room temperature and is soluble in polar solvents due to the amino group, which can engage in hydrogen bonding. It is often used in organic synthesis and may serve as an intermediate in the production of pharmaceuticals or other chemical entities. The compound's molecular structure allows for various functionalizations, making it a versatile building block in medicinal chemistry. Additionally, 5-Aminoindan-1-one may exhibit interesting pharmacological properties, although specific biological activities would depend on further research and context. Safety data should be consulted for handling and usage, as with any chemical substance.

5-Aminoindan-1-one

3470-54-0: 5-Amino-1-oxoindane, 5-amino-2,3-dihydro-1H-inden-1-one, 5-Amino-1-Indanone

5-Aminoindan-1-one is a hydroxy group with a potent inhibitory activity. It is an active methylene that can be synthesized by the reaction of formaldehyde and acetone. 5-Aminoindan-1-one has been shown to have photophysical properties, such as fluorescence, phosphorescence and chemiluminescence. This molecule has significant cytotoxicity against various cancer cells, including carcinoma cells. The inhibition mechanism of 5-aminoindan-1-one is not yet fully understood, but it may be due to its ability to inhibit cholinesterases and inhibit the synthesis of glucose from glycogen in hypoglycemic conditions.

CAS 3470-54-0: 5-Aminoindan-1-one

5-Aminoindan-1-one

Ref: 3D-FA152531

5-aminoindan-1-one

Ref: IN-DA0035VW

5-Amino-1-indanone

Ref: 10-F038571

5-Aminoindan-1-one

Ref: 54-OR26184