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Cyclohexanone oxime iminoxyl radical, also known as "Cyclohexanon-oxim-iminoxy-radikal," is a chemical species derived from cyclohexanone oxime, which is an organic compound with the formula C6H11NO. This radical is formed when a hydrogen atom is abstracted from the oxime group, resulting in a highly reactive species with an unpaired electron. It plays a crucial role in various chemical reactions, such as the Beckmann rearrangement, where it undergoes a transformation to form an amide. The iminoxyl radical is also involved in the oxidation of aldoximes to nitrile oxides, which are important intermediates in organic synthesis. Due to its reactivity, it is often generated and utilized under controlled conditions to prevent unwanted side reactions.

6146-76-5

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6146-76-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6146-76-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,4 and 6 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6146-76:
(6*6)+(5*1)+(4*4)+(3*6)+(2*7)+(1*6)=95
95 % 10 = 5
So 6146-76-5 is a valid CAS Registry Number.

6146-76-5Downstream Products

6146-76-5Relevant academic research and scientific papers

Indirect Detection of Carbenes by Electron Spin Resonance: Triplet Trapping

Forrester, Alexander R.,Sadd, John S.

, p. 1273 - 1278 (2007/10/02)

Transient triplet carbenes have been converted into relatively long-lived iminoxyls by reaction with nitric oxide and hence been detected indirectly by e.s.r. spectroscopy.The process is formally analogous to spin trapping of monoradicals by nitrones and nitroso-compounds.Triplet nitrenes could not be trapped in this way.

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