1-(2,4-Dinitrophenyl)aziridine is a chemical compound characterized by its aziridine ring, which is a three-membered cyclic amine. The presence of a 2,4-dinitrophenyl group introduces significant electron-withdrawing characteristics due to the nitro groups, which can influence the compound's reactivity and stability. This compound is typically a yellow crystalline solid, reflecting the dinitrophenyl moiety's strong chromophoric properties. It is known for its potential use in organic synthesis, particularly in the formation of more complex molecules through nucleophilic substitution reactions. The aziridine ring can undergo ring-opening reactions, making it a versatile intermediate in synthetic chemistry. However, due to the presence of the dinitrophenyl group, it may also exhibit heightened sensitivity to heat and shock, necessitating careful handling. Additionally, the compound's toxicity and environmental impact should be considered, as dinitrophenyl derivatives are often associated with hazardous properties. Overall, 1-(2,4-dinitrophenyl)aziridine serves as an important building block in various chemical applications, particularly in the fields of medicinal chemistry and materials science.

1-(2,4-dinitrophenyl)aziridine

27141-65-7: 1-(2,4-Dinitrophenyl)aziridine is a chemical compound characterized by its aziridine ring, which is a three-membered cyclic amine. The presence of a 2,4-dinitrophenyl group introduces significant electron-withdrawing characteristics due to the nitro groups, which can influence the compound's reactivity and stability. This compound is typically a yellow crystalline solid, reflecting the dinitrophenyl moiety's strong chromophoric properties. It is known for its potential use in organic synthesis, particularly in the formation of more complex molecules through nucleophilic substitution reactions. The aziridine ring can undergo ring-opening reactions, making it a versatile intermediate in synthetic chemistry. However, due to the presence of the dinitrophenyl group, it may also exhibit heightened sensitivity to heat and shock, necessitating careful handling. Additionally, the compound's toxicity and environmental impact should be considered, as dinitrophenyl derivatives are often associated with hazardous properties. Overall, 1-(2,4-dinitrophenyl)aziridine serves as an important building block in various chemical applications, particularly in the fields of medicinal chemistry and materials science.

CAS 27141-65-7

1-(2,4-dinitrophenyl)aziridine

Aloenin

Ref: 54-BUP20793

CB 1837

Ref: TM-T30759