31970-06-6

Usage

Nitro compound

A type of organic compound that contains a nitro group (-NO2), which is known for its explosive properties and is commonly used in the synthesis of other organic compounds.

Cyclohexane ring

A six-carbon ring structure in the molecule, which is a cyclic alkane with the formula C6H12.

tert-Butyl group

A type of alkyl group with the formula (CH3)3C, which is attached to the cyclohexane ring in 1-tert-butyl-4-nitrocyclohexane.

Yellow crystalline solid

The physical appearance of the compound, which is a yellow, crystalline solid with a slightly sweet odor.

Stable under normal conditions

The compound is considered to be stable and does not readily undergo chemical reactions or decomposition under standard temperature and pressure.

Health hazards

1-tert-butyl-4-nitrocyclohexane may pose potential health risks, so it should be handled with care and proper safety precautions.

Storage

The compound should be stored in a cool, dry place away from incompatible materials to maintain its stability and prevent any hazardous reactions.

Upstream product

• 75107-61-8 4-tert-butyl-1-chloro-1-nitrocyclohexane 
• 82992-54-9 c-4-t-butyl-r-1-chloro-1-nitrocyclohexane 
• 82992-53-8 trans-4-t-butyl-1-chloro-1-nitrocyclohexane 
• 5451-55-8 4-tert-butylcyclohexanecarboxylic acid 
• 923947-85-7 4-tert-butyl-1-chloro-1-nitrosocyclohexane 
• 4701-98-8 4-tert-butylcyclohexanone oxime 
• 5400-88-4 4-tert-butylcyclohexylamine 

Downstream Products

• 89023-71-2 trans-4-(tert-butyl)-1-nitrocyclohexylmethyl acetate 
• 344236-90-4 1-(4-tert-Butyl-1-phenylsulfanyl-cyclohexyl)-4-nitro-benzene 
• 82992-62-9 t-4-t-butyl-r-1-(1-methyl-1-nitroethyl)-1-(p-nitrophenyl) cyclohexane 
• 82992-63-0 2--2-ethilmalononitrile 
• 82992-61-8 r-1-benzenesulfonyl-t-4-t-butyl-1-(p-nitrophenyl)-cyclohexane 
• 82992-60-7 r-1-benzenesulfonyl-c-4-t-butyl-1-(p-nitrophenyl)-cyclohexane 
• 82992-58-3 t-4-t-butyl-1-(p-nitrophenyl)-r-1-p-toluenesulfonylcyclohexane 
• 82992-59-4 c-4-t-butyl-1-(p-nitrophenyl)-r-1-p-toluenesulfonylcyclohexane 
• 177174-04-8 C₁₀H₁₈⁽¹⁸⁾O 
• 98-53-3 4-tercbutyl-cyclohexanone 
• 85204-31-5 4-(tert-butyl)cyclohexylmethyl acetate 
• 19461-34-8 cis-4-(tert-butyl)cyclohexylmethyl acetate 
• 19461-35-9 trans-4-(tert-butyl)cyclohexylmethyl acetate 
• 10601-39-5 trans-(4-tert-butyl-cyclohexyl)-methanol 

Relevant academic research and scientific papers

Zirconium-Catalyzed Oxidation of Primary Aliphatic Amines to Nitro Compounds with tert-Butyl Hydroperoxide

Primary aliphatic amines are oxidized with tert-butyl hydroperoxide to the corresponding nitro compounds in 50-98% yield using Zr(Ot-Bu)4 as the catalyst. The CH-acidic nitro compounds are not epimerized under these reaction conditions.

THE STEREOCHEMISTRY OF THE SRN1 REACTION IN SOME CYCLOHEXANE DERIVATIVES

The substitution reactions of nitrocyclohexanes 8, 9, 12 and 23 with various nucleophiles were sudied and were found to proceed by the electron-transfer initiated SRN1 mechanism.Epimeric products were formed and the proportion of epimers under

AN EFFECTIVE AND MILD METHOD FOR THE CONVERSION OF OXIMES TO SECONDARY NITRO COMPOUNDS

A mild and efficient process for the conversion of cyclic ketones to staurated nitro compounds, as outlined in eq. 1 below, is described.