2,6-DIISOPROPYLNAPHTHALENE

Химические свойства

beige crystalline platelets

Общее описание

Clear yellowish brown liquid with a faint sweet odor.

Реакции воздуха и воды

Insoluble in water.

Профиль реактивности

Vigorous reactions, sometimes amounting to explosions, can result from the contact between aromatic hydrocarbons, such as 2,6-DIISOPROPYLNAPHTHALENE, and strong oxidizing agents. They can react exothermically with bases and with diazo compounds. Substitution at the benzene nucleus occurs by halogenation (acid catalyst), nitration, sulfonation, and the Friedel-Crafts reaction. Friedel-Crafts acylation of naphthalene using benzoyl chloride, catalyzed by AlCl3, must be conducted above the melting point of the mixture, or the reaction may be violent [Clar, E. et al., Tetrahedron, 1974, 30, 3296].

Угроза здоровью

Exposure can cause irritation of eyes, nose and throat.

Пожароопасность

Special Hazards of Combustion Products: Irritating vapors and toxic gases, such as carbon dioxide and carbon monoxide, may be formed when involved in fire.