2-Acetyl-4-nitroindane-1, identified by its CAS number 25125-04-6, is an organic compound that belongs to the class of indane derivatives. This substance features a nitro group and an acetyl group attached to the indane structure, which contributes to its unique chemical properties. Typically, compounds of this nature exhibit moderate to high stability under standard conditions, but their reactivity can vary based on the functional groups present. The nitro group is known for its electron-withdrawing properties, which can influence the compound's reactivity in electrophilic substitution reactions. Additionally, the acetyl group can participate in various chemical transformations, such as nucleophilic attacks or condensation reactions. 2-Acetyl-4-nitroindane-1 may also exhibit interesting biological activities, making it a subject of interest in medicinal chemistry. Its solubility, melting point, and other physical properties would depend on the specific conditions and purity of the sample. Overall, this compound represents a versatile structure with potential applications in organic synthesis and pharmaceuticals.

2-Acetyl-4-nitroindane-1

25125-04-6: 2-Acetyl-4-nitroindane-1,3-dione, 2-acetyl-4-nitro-1H-indene-1,3(2H)-dione

1H-Indene-1,3(2H)-dione, 2-acetyl-4-nitro-

2-Acetyl-4-nitroindane-1,3-dione

2-Acetyl-4-nitroindane-1,3-dione is a synthetic compound that is assembled in two steps from commercially available starting materials. The first step involves the assembly of the nitro group and acetyl group on the indane ring. The second step involves the oxidative cyclization of the nitro group to form the final product. The compound was monitored by UV absorption and HPLC analysis with a spermidine standard. It has been shown to selectively inhibit trypanothione reductase, an enzyme involved in trypanosome metabolism. 2-Acetyl-4-nitroindane-1,3-dione is also an analogue of disulphide, which has been shown to be effective against trypanosomes. 2-Acetyl-4-nitroindane-1,3-dione is synthesized on solid phase using strategies developed for peptides and amines. This compound has also

CAS 25125-04-6: 2-Acetyl-4-nitroindane-1

1H-Indene-1,3(2H)-dione, 2-acetyl-4-nitro-

Ref: IN-DA002QJQ

2-Acetyl-4-nitroindane-1,3-dione

Ref: 54-OR018931

2-Acetyl-4-nitroindane-1,3-dione

Ref: 3D-FA66807