N-(2-chloroethyl)phthalimide is an organic compound characterized by its phthalimide structure, which is a cyclic imide derived from phthalic acid. It features a chloroethyl group attached to the nitrogen atom of the imide, contributing to its reactivity. This compound is typically a white to off-white solid and is soluble in organic solvents such as acetone and chloroform, but has limited solubility in water. N-(2-chloroethyl)phthalimide is primarily used in organic synthesis, particularly as an intermediate in the production of various pharmaceuticals and agrochemicals. Its reactivity is influenced by the presence of the chloroethyl group, which can participate in nucleophilic substitution reactions. Additionally, it may exhibit biological activity, making it of interest in medicinal chemistry. Safety precautions should be taken when handling this compound, as it may pose health risks due to its potential toxicity and reactivity. Proper storage and disposal methods are essential to mitigate environmental impact and ensure safety in laboratory settings.

N-(2-chloroethyl)phthalimide

6270-06-0: N-(2-chloroethyl)phthalimide is an organic compound characterized by its phthalimide structure, which is a cyclic imide derived from phthalic acid. It features a chloroethyl group attached to the nitrogen atom of the imide, contributing to its reactivity. This compound is typically a white to off-white solid and is soluble in organic solvents such as acetone and chloroform, but has limited solubility in water. N-(2-chloroethyl)phthalimide is primarily used in organic synthesis, particularly as an intermediate in the production of various pharmaceuticals and agrochemicals. Its reactivity is influenced by the presence of the chloroethyl group, which can participate in nucleophilic substitution reactions. Additionally, it may exhibit biological activity, making it of interest in medicinal chemistry. Safety precautions should be taken when handling this compound, as it may pose health risks due to its potential toxicity and reactivity. Proper storage and disposal methods are essential to mitigate environmental impact and ensure safety in laboratory settings.

CAS 6270-06-0

N-(2-chloroethyl)phthalimide

2-(2-chloroethyl)-1H-isoindole-1,3(2H)-dione

Ref: 10-F366495

N-(2-Chloroethyl)phthalimide

Ref: IN-DA003ERB

2-(2-Chloroethyl)-1H-isoindole-1,3(2H)-dione

Ref: 54-OR55253