21460-40-2

Usage

Uses

Used in Dye Production:
Benzene, 1-methyl-4-(1-methylethyl)-2,5-dinitrosois used as an intermediate in the synthesis of various dyes. Its unique chemical structure allows for the formation of different colored compounds, making it a valuable component in the dye industry.
Used in Pharmaceutical Production:
This chemical compound is also utilized in the production of certain pharmaceuticals. Its reactivity enables the formation of various drug molecules with potential therapeutic effects.
Used in Combustion Processes:
Benzene, 1-methyl-4-(1-methylethyl)-2,5-dinitrosois commonly found as a byproduct of combustion processes, including vehicle emissions and tobacco smoke. While its presence in these processes is not intentional, it highlights the compound's reactivity and potential environmental impact.
Health and Safety Considerations:
Due to its highly reactive and toxic nature, exposure to Benzene, 1-methyl-4-(1-methylethyl)-2,5-dinitrosocan cause a range of health effects, including irritation of the eyes, skin, and respiratory system. Additionally, there are potential carcinogenic effects associated with exposure to this chemical. Therefore, it is crucial to implement proper handling and safety measures when dealing with Benzene, 1-methyl-4-(1-methylethyl)-2,5-dinitroso- to minimize health risks and environmental impact.

Upstream product

• 490-91-5 thymoquinone 
• 74317-48-9 2-isopropyl-5-methyl-p-benzoquinone dioxime 

Downstream Products

• 127368-16-5 2-isopropyl-5-methyl-p-dinitrobenzene 

Relevant academic research and scientific papers

Catalytic Autoxidation of Benzoquinone Dioximes with Nitrogen Oxides: Steric Effects on the Preparation of Monomeric Dinitrosobenzenes

A convenient catalytic method for the autoxidation of quinone dioximes to dinitrosobenzenes with dioxygen is based on the presence of small amounts of nitrogen oxides.The catalytic cycle is deduced from the facile chemical oxidation of quinone dioxime to dinitrobenzene with stoichiometric amounts of the 1-electron oxidant, nitrosonium-either as the NO+BF4- salt or the disproportionated ion pair NO+NO3- derived from nitrogen dioxide.The regeneration of NO+ occurs by the subsequent oxidation of nitric oxide (NO) with dioxygen to nitrogen dioxide followed by the disproportionation to nitrosonium nitrate in the presence of electron-rich donors.Indeed, dioximes of various p-benzoquinones are shown to be strong reducing agents by transient electrochemistry.Electrochemical oxidation also leads to dinitrosobenzenes in good yields at anodic potentials of ca. 1.3 V.The substitution of p-dinitrosobenzene with bulky alkyl groups stabilizes the monomeric form, which is otherwise extensively associated.

Properties and Spectroscopic Studies of Substituted 1,4-Dinitrosobenzenes.

Spectroscopic studies of three substituted dinitrosobenzenes show that in the solid state the compounds are long chain and based upon the N2O2 group.Depolymerisation to the monomer unit (substituted benzenes containing two monomeric N=O groups) occurs on heating, on vaporisation and on dissolution in organic solvents.The previously reported tetrachloro- and tetrabromodinitrosobenzenes could not be confirmed , the product in each case being the tetrahalogenonitrosoaniline.