17355-89-4 Usage
Description
Hydroperoxide, 1-methyl-1-(2-naphthalenyl)ethyl is an organic compound characterized by the presence of a hydroperoxide functional group, a methyl group, and a naphthalene ring. This unique structure endows it with specific chemical properties that make it valuable in various industrial applications.
Uses
Used in Polymer Industry:
Hydroperoxide, 1-methyl-1-(2-naphthalenyl)ethyl is used as a radical initiator for polymerization reactions, specifically in the production of polystyrene and polyethylene. Its role in initiating the polymerization process is crucial for creating these widely used plastics.
Used in Chemical Synthesis:
As an oxidizing agent, Hydroperoxide, 1-methyl-1-(2-naphthalenyl)ethyl is utilized in various chemical synthesis processes. Its ability to accept electrons and form new chemical bonds makes it a versatile component in the synthesis of different compounds.
Used in Fragrance and Flavor Industry:
Hydroperoxide, 1-methyl-1-(2-naphthalenyl)ethyl is employed in the production of fragrances and flavors due to its reactive nature and potential to contribute to the formation of desired aromatic compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 17355-89-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,3,5 and 5 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 17355-89:
(7*1)+(6*7)+(5*3)+(4*5)+(3*5)+(2*8)+(1*9)=124
124 % 10 = 4
So 17355-89-4 is a valid CAS Registry Number.
17355-89-4Relevant articles and documents
Efficient and selective oxidation of tertiary benzylic C[sbnd]H bonds with O2 catalyzed by metalloporphyrins under mild and solvent-free conditions
Hu, Meng-Yun,Liu, Lei,Qi, Bei,She, Yuan-Bin,Shen, Hai-Min,Ye, Hong-Liang
, (2020/05/19)
The direct and efficient oxidation of tertiary benzylic C[sbnd]H bonds to alcohols with O2 was accomplished in the presence of metalloporphyrins as catalysts under solvent-free and additive-free conditions. Based on effective inhibition on the unselective autoxidation and deep oxidation, systematical investigation on the effects of porphyrin ligands and metal centers, and apparent kinetics study, the oxidation system employing porphyrin manganese(II) (T(2,3,6-triCl)PPMn) with bulkier substituents as catalyst, was regarded as the most promising and efficient one. For the typical substrate, the conversion of cumene could reach up to 57.6% with the selectivity of 70.5% toward alcohol, both of them being higher than the current documents under similar conditions. The superiority of T(2,3,6-triCl)PPMn was mainly attributed to its bulkier substituent groups preventing metalloporphyrins from oxidative degradation, its planar structure favoring the interaction between central metal with reactants, and the high efficiency of Mn(II) in the catalytic transformation of hydroperoxides to alcohols.
