N-(8-Bromooctyl)phthalimide is an organic compound characterized by its phthalimide structure, which is a cyclic imide derived from phthalic acid. This compound features a brominated octyl chain, specifically an 8-bromooctyl group, which contributes to its hydrophobic properties and influences its reactivity. It is typically a white to off-white solid at room temperature and is soluble in organic solvents such as dichloromethane and acetone, but has limited solubility in water. The presence of the bromine atom enhances its potential as a reactive intermediate in various chemical reactions, including nucleophilic substitutions. N-(8-Bromooctyl)phthalimide is often utilized in organic synthesis, particularly in the preparation of surfactants, polymers, and other functional materials. Additionally, its unique structure allows for applications in medicinal chemistry and materials science. Safety precautions should be observed when handling this compound, as it may pose health risks if ingested or inhaled, and appropriate personal protective equipment should be used.

N-(8-Bromooctyl)phthalimide

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1H-Isoindole-1,3(2H)-dione, 2-(8-bromooctyl)-

2-(8-Bromooctyl)isoindoline-1,3-dione is a chelating agent that can be used as an intermediate in the synthesis of propyl bromoacetate. It is synthesized by the dialkylation of 2-(propyl)isoindoline-1,3-dione with bromoacetyl chloride. The resulting product is hydrolyzed by triethylamine to yield the desired product. This compound has been shown to form a chelate with metal ions such as zinc and copper. 2-(8-Bromooctyl)isoindoline-1,3-dione also reacts with aminopropyl dglucose to give a functionalized product.

CAS 17702-83-9: N-(8-Bromooctyl)phthalimide

1H-Isoindole-1,3(2H)-dione, 2-(8-bromooctyl)-

Ref: IN-DA00253B

N-(8-Bromooctyl)phthalimide

Ref: 10-F018143

2-(8-Bromooctyl)isoindoline-1,3-dione

Ref: 3D-SAA70283