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.
Check Digit Verification of cas no
The CAS Registry Mumber 31970-06-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,9,7 and 0 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 31970-06:
(7*3)+(6*1)+(5*9)+(4*7)+(3*0)+(2*0)+(1*6)=106
106 % 10 = 6
So 31970-06-6 is a valid CAS Registry Number.
31970-06-6Relevant articles and documents
Zirconium-Catalyzed Oxidation of Primary Aliphatic Amines to Nitro Compounds with tert-Butyl Hydroperoxide
Krohn, Karsten,Kuepke, Jochen
, p. 679 - 682 (2007/10/03)
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
Corey, E. J.,Estreicher, Herbert
, p. 1117 - 1120 (2007/10/02)
A mild and efficient process for the conversion of cyclic ketones to staurated nitro compounds, as outlined in eq. 1 below, is described.