2,4,6-Tri-tert-butylnitrosobenzene is an organic compound characterized by its nitroso group (-NO) attached to a benzene ring that is further substituted with three tert-butyl groups at the 2, 4, and 6 positions. This structure contributes to its significant steric hindrance and hydrophobic nature, making it relatively insoluble in water but soluble in organic solvents. The presence of the nitroso group imparts unique reactivity, allowing it to participate in various chemical reactions, including those typical of nitroso compounds, such as nucleophilic attacks and reduction reactions. The tert-butyl groups enhance the compound's stability and influence its physical properties, such as melting and boiling points. Additionally, 2,4,6-Tri-tert-butylnitrosobenzene is of interest in research contexts, particularly in studies related to nitroso compounds and their applications in organic synthesis and materials science. Safety precautions should be observed when handling this compound due to potential toxicity associated with nitroso compounds.

2,4,6-Tri-tert-butylnitrosobenzene

24973-59-9: 1,3,5-Tris(1,1-dimethylethyl)-2-nitrosobenzene, 1,3,5-Tritert-butyl-2-nitrosobenzene, 1-Nitroso-2,4,6-tri-t-butylbenzene, 2,4,6-Tri-tert-butyl-1-nitrosobenzene, 2,4,6-Tri-tert-butylnitrosobenzene, Benzene, 1,3,5-tri-tert-butyl-2-nitroso-, Benzene, 1,3,5-tris(1,1-dimethylethyl)-2-nitroso-, Nsc 677542, 1,3,5-Tri(tert-butyl)-2-nitrosobenzene

2,4,6-Tri-tert-butylnitrosobenzene is a research chemical with various applications. It can be used to study the interaction between ganglioside GM2 and other compounds. This compound is also commonly used in electrode fabrication for its excellent electrical conductivity properties. Additionally, 2,4,6-Tri-tert-butylnitrosobenzene has been found to have potential as an intermediate in the synthesis of diclofenac, a nonsteroidal anti-inflammatory drug. Its benzylic reactivity makes it useful in the development of pyrazosulfuron herbicides. Furthermore, this compound can be utilized in the production of antibodies due to its ability to conjugate with phosphoric groups. Its water-soluble nature makes it suitable for various applications in different fields such as pharmaceuticals (e.g., cefpodoxime proxetil), fatty acid synthesis, cellulose modification, and enhancing bioavailability of certain compounds

CAS 24973-59-9: 2,4,6-Tri-tert-butylnitrosobenzene

2,4,6-Tri-tert-butylnitrosobenzene

Ref: 3D-ZAA97359

Benzene, 1,3,5-tris(1,1-dimethylethyl)-2-nitroso-

Ref: IN-DA002Q26

2,4,6-Tri-tert-butylnitrosobenzene

Ref: 3B-T1534