31970-06-6

Basic information

• Product Name: 1-tert-butyl-4-nitrocyclohexane
• CAS NO: 31970-06-6
• Molecular Formula: C₁₀H₁₉NO₂
• Molecular Weight: 185.2634
• Mol File: 31970-06-6.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 253.9°C at 760 mmHg
• Flash Point: 93.9°C
• Density: 0.97g/cm³
• Vapor Pressure: 0.0177mmHg at 25°C
• Refractive Index: 1.464
• CAS DataBase Reference: 1-tert-butyl-4-nitrocyclohexane(CAS DataBase Reference)
• NIST Chemistry Reference: 1-tert-butyl-4-nitrocyclohexane(31970-06-6)
• EPA Substance Registry System: 1-tert-butyl-4-nitrocyclohexane(31970-06-6)

Safety Data

• Hazardous Substances Data: 31970-06-6(Hazardous Substances Data)

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 
• 5400-88-4 4-tert-butylcyclohexylamine 
• 5451-55-8 4-tert-butylcyclohexanecarboxylic acid 
• 4701-98-8 4-tert-butylcyclohexanone oxime 
• 923947-85-7 4-tert-butyl-1-chloro-1-nitrosocyclohexane 

Downstream Products

• 78928-45-7 c-4-t-butyl-r-1-nitro-1-(p-nitrophenyl)cyclohexane 
• 89023-71-2 trans-4-(tert-butyl)-1-nitrocyclohexylmethyl acetate 
• 13004-06-3 cis-(4-tert-butylcyclohexyl)methanol 
• 10601-39-5 trans-(4-tert-butyl-cyclohexyl)-methanol 
• 19461-35-9 trans-4-(tert-butyl)cyclohexylmethyl acetate 
• 19461-34-8 cis-4-(tert-butyl)cyclohexylmethyl acetate 
• 85204-31-5 4-(tert-butyl)cyclohexylmethyl 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 

Relevant articles and documents

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.

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.