N-(4-Ethylphenyl)maleimide is an organic compound characterized by its maleimide structure, which features a five-membered ring containing a carbonyl and a nitrogen atom. This compound is typically a white to light yellow solid at room temperature and is known for its reactivity, particularly in Michael addition reactions due to the presence of the maleimide double bond. It exhibits good thermal stability and is soluble in organic solvents such as acetone and dichloromethane, but is less soluble in water. The presence of the ethylphenyl group enhances its hydrophobic properties and can influence its reactivity and interaction with other chemical species. N-(4-Ethylphenyl)maleimide is often utilized in polymer chemistry, particularly in the synthesis of various copolymers and as a crosslinking agent in thermosetting resins. Additionally, it may find applications in the field of materials science and organic electronics due to its unique structural features and functional properties. Safety precautions should be taken when handling this compound, as it may pose health risks upon exposure.

N-(4-Ethylphenyl)maleimide

76620-00-3: N-(4-Ethylphenyl)maleimide is an organic compound characterized by its maleimide structure, which features a five-membered ring containing a carbonyl and a nitrogen atom. This compound is typically a white to light yellow solid at room temperature and is known for its reactivity, particularly in Michael addition reactions due to the presence of the maleimide double bond. It exhibits good thermal stability and is soluble in organic solvents such as acetone and dichloromethane, but is less soluble in water. The presence of the ethylphenyl group enhances its hydrophobic properties and can influence its reactivity and interaction with other chemical species. N-(4-Ethylphenyl)maleimide is often utilized in polymer chemistry, particularly in the synthesis of various copolymers and as a crosslinking agent in thermosetting resins. Additionally, it may find applications in the field of materials science and organic electronics due to its unique structural features and functional properties. Safety precautions should be taken when handling this compound, as it may pose health risks upon exposure.

CAS 76620-00-3

N-(4-Ethylphenyl)maleimide

N-(4-Ethylphenyl)maleimide

Ref: IN-DA003SCG

1-(4-ethylphenyl)-1H-pyrrole-2,5-dione

Ref: 10-F371787