112092-00-9 Usage
General Description
2-(1-trifluoromethyl-2-nitroethyl)cyclohexanone is a chemical compound with the molecular formula C10H14F3NO3. It is a yellow to orange crystalline solid and is classified as a ketone. 2-(1-TRIFLUOROMETHYL-2-NITROETHYL)CYCLOHEXANONE is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. It has potential applications in the field of organic chemistry and can be used as a building block for the synthesis of more complex molecules. The presence of both nitro and trifluoromethyl groups in the compound makes it a versatile starting material for the production of a wide range of organic compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 112092-00-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,0,9 and 2 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 112092-00:
(8*1)+(7*1)+(6*2)+(5*0)+(4*9)+(3*2)+(2*0)+(1*0)=69
69 % 10 = 9
So 112092-00-9 is a valid CAS Registry Number.
112092-00-9Relevant academic research and scientific papers
New functionalized, differently fluorinated building-blocks via Michael addition to γ-fluoro-α-nitroalkenes
Molteni, Marco,Consonni, Roberto,Giovenzana, Tommaso,Malpezzi, Luciana,Zanda, Matteo
, p. 901 - 908 (2008/02/10)
The Michael addition of ketone-derived enamines, metalated methylene active compounds and N-methyl pyrroles to γ-fluoro-α-nitroalkenes provided in moderate to good isolated yields the corresponding β-fluoroalkyl nitro compounds, which represent new intere
REACTION OF 1,1,1-TRIFLUORO-2-DIAZO-3-NITROPROPANE WITH THE ENAMINES OF KETONES
Aizikovich, A. Ya.,Korotaev, V. Yu.,Yaroslavtseva, L. E.
, p. 1045 - 1047 (2007/10/02)
The reaction of 1,1,1-trifluoro-2-diazo-3-nitropropane with the enamines of ketones leads to the insertion of 1-trifluoromethyl-1-nitromethylcarbene at the olefinic C-H bond.The structure of the insertion products and of the fluorine-containing γ-nitro ketones formed after hydrolysis was established by 1H and 19F NMR spectra.
