1H-Isoindole-1,3(2H)-dione, 2-(2-bromoethyl)- [ACD/Index Name]
2-(2-Bromethyl)-1H-isoindol-1,3(2H)-dion [German] [ACD/IUPAC Name]
2-(2-Bromoethyl)-1H-isoindole-1,3(2H)-dione [ACD/IUPAC Name]
2-(2-Bromoéthyl)-1H-isoindole-1,3(2H)-dione [French] [ACD/IUPAC Name]
Phthalimide, N- (2-bromoethyl)-
Phthalimide, N-(2-bromoethyl)- (8CI)
Benzoic acid, 4-(aminomethyl)- (9CI)
N-(2-Bromoethyl) Phthalimide (en)
Beilstein Registry Number
Off white crystalline powder
Specifications and Other Information of Our
Store in room temperature for long time; Protect from light.
N-(2-Bromoethyl)phthalimide used in Pharmaceutical Intermediates，
is a chemical compound that has shown to have a range of useful properties in various applications. This compound belongs to the family of phthalimide derivatives and is widely used as an intermediate in organic synthesis.
One of the most significant applications of N-(2-bromoethyl)phthalimide is its use in the synthesis of biologically active compounds. It has been used to synthesize a variety of biologically active molecules, including antitumor and antibacterial agents. N-(2-bromoethyl)phthalimide has been found to be an effective reagent in the synthesis of several novel compounds that possess a wide range of biological activities.
In addition to its biological applications, N-(2-bromoethyl)phthalimide has also found use as a cross-linking agent in the preparation of polymers. It has been shown to be an effective cross-linking agent for a range of polymers, including poly(vinyl alcohol) and poly(acrylic acid). The resulting cross-linked polymers have improved mechanical properties and thermal stability, making them suitable for a range of applications.
Another important application of N-(2-bromoethyl)phthalimide is in the field of materials science. It has been used as a surface modifier for a range of materials, including glass, metals, and polymers. The resulting modified surfaces exhibit improved adhesion, wettability, and durability, making them suitable for a range of applications in the fields of electronics, optics, and coatings.
General View of Documents
HPLC of N-(2-Bromoethyl)phthalimide CAS 574-98-1
HNMR of N-(2-Bromoethyl)phthalimide CAS 574-98-1
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