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α-(2-Acetoxy-2,6-di-tert-butyl-1-oxo-3,5-cyclohexadienyl)-N-tert-butylnitron is a complex organic compound with the molecular formula C20H29NO4. It is characterized by a nitron group (a type of nitroso compound) attached to a cyclohexadienyl ring, which is further substituted with acetoxy, tert-butyl, and oxo groups. α-(2-Acetoxy-2,6-di-tert-butyl-1-oxo-3,5-cyclohexadienyl)-N-tert-butylnitron is known for its antioxidant properties and is used in the stabilization of polymers, particularly in the rubber and plastics industry, to prevent degradation caused by heat, light, and oxygen. Its structure provides it with the ability to scavenge free radicals, thereby protecting materials from oxidative damage.

93214-35-8

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93214-35-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93214-35-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,2,1 and 4 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 93214-35:
(7*9)+(6*3)+(5*2)+(4*1)+(3*4)+(2*3)+(1*5)=118
118 % 10 = 8
So 93214-35-8 is a valid CAS Registry Number.

93214-35-8Relevant academic research and scientific papers

Reactions of the 2,6-Di-tert-butyl-4-(N-tert-butylnitrono)-phenoxyl Radical

Schulz, Manfred,Bach, Barbara,Reinhardt, Michael

, p. 579 - 587 (2007/10/02)

The title compound, a phenoxyl radical containing a nitrono group, reacts with alcohols and tert-butylhydroperoxide yielding phenol and products of secondary solvent reactions.The reactions with lead tetraacetate, tert.-butoxy and 2-cyanoisopropyl radicals give high yields of cyclohexadienone adducts (6, 7 and 10) containing unchanged nitrono function.The reaction with dibenzoylperoxide, however, leads to the modification of the nitrono group yielding the N-benzoyloxycarboxamide (8).In the acidic decomposition of the tert-butoxy radical adduct we suggest a nitrenium ion (16) as an intermediate.

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