59368-15-9

Usage

Physical state

Colorless liquid the compound appears as a colorless liquid, which means it does not have a distinct color and flows like a fluid.

Primary use

Intermediate in organic synthesis 1-Methyl-1-nitrocyclohexane is mainly used as a chemical intermediate, which means it is a starting material or a product formed during the synthesis of more complex organic compounds.

Reagent application

Manufacture of chemicals and pharmaceuticals the compound serves as a reagent, or a chemical substance used in chemical reactions, to produce other chemicals and pharmaceuticals.

Industrial use

Production of rubber and plastic products 1-Methyl-1-nitrocyclohexane can be used in the production of rubber and plastic products, indicating its versatility in various industries.

Toxic nature

Irritating and toxic the compound is known for its irritating and toxic properties, which can cause harm to humans and the environment if not handled properly.

Hazardous decomposition

Releases toxic fumes when heated when 1-Methyl-1-nitrocyclohexane is heated to decomposition, it can release toxic fumes, making it crucial to handle with caution and under controlled conditions.

Upstream product

• 82166-21-0 methyl cyclohexane 
• 7697-37-2 nitric acid 
• 60-29-7 diethyl ether 
• 5469-33-0 cyclohexylmethyl iodide 
• 590-67-0 1-Methylcyclohexanol 
• 6526-78-9 1-methyl-1-cyclohexylamine 

Downstream Products

• 6526-78-9 1-methyl-1-cyclohexylamine 
• 42066-84-2 N-<1-Methyl-cyclohexyl>-hydroxylamin 
• 68896-31-1 1-methylcyclohexane-1-thiol 
• 53635-21-5 dimethyl-(1-methyl-cyclohexyl)-amine 
• 114035-89-1 methyl-(1-methyl-cyclohexyl)-amine 
• 345252-04-2 benzyl-(1-methyl-cyclohexyl)-amine 
• 109436-34-2 1,1'-Dimethyl-azoxycyclohexan 
• 110-15-6 succinic acid 
• 144-62-7 oxalic acid 

Relevant academic research and scientific papers

NITRATED HYDROCARBONS, DERIVATIVES, AND PROCESSES FOR THEIR MANUFACTURE

Provided is a process for the formation of nitrated compounds by the nitration of hydrocarbon compounds with dilute nitric acid. Also provided are processes for preparing industrially useful downstream derivatives of the nitrated compounds, as well as novel nitrated compounds and derivatives, and methods of using the derivatives in various applications.

PROCESS FOR THE PREPARATION OF NITRO COMPOUNDS AND METHOD FOR THE REMOVAL OF NITROGEN DIOXIDE

In the invented process for producing a nitro compound, an organic substrate and nitrogen dioxide are reacted in the presence of oxygen or are reacted in a molar ratio of nitrogen dioxide to the organic substrate of less than 1 to yield a corresponding nitro compound. The reaction may be performed in the presence of N-hydroxyphthalimide or other imide compounds. Such organic substrates include (a) aliphatic hydrocarbons, (b) alicyclic hydrocarbons, (c) non-aromatic heterocyclic compounds each having a carbon atom on a ring, which carbon atom is bonded to a hydrogen atom, (d) compounds each having a carbon-hydrogen bond at the adjacent position to an aromatic ring, and (e) compounds each having a carbon-hydrogen bond at the adjacent position to a carbonyl group. This process can efficiently nitrate an organic substrate even under relatively mild conditions.

A simple and highly efficient procedure for the preparation of aliphatic nitro compounds directly from alcohols

A simple and highly efficient one-pot synthesis of aliphatic nitro compounds from the corresponding alcohols with NaNO2-AcOH-HCl system is described.