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1-oxo-2-(+)-α-methylbenzyl-3-hydroperoxy-3-phenylisoindole is a complex organic compound with a molecular formula of C21H17NO3. It is characterized by the presence of an isoindole ring system, which is a tricyclic structure consisting of a benzene ring fused to a pyrrolidine ring. The molecule features a hydroperoxy group (-OOH), an α-methylbenzyl group (-CH2-C6H5-CH3), and a phenyl group (-C6H5) attached to the isoindole core. The compound exhibits a chiral center at the α-methylbenzyl group, which is in the (+)-α configuration, indicating that it is the R-enantiomer. This chemical is synthesized through a series of reactions involving the isoindole core and the subsequent introduction of the functional groups. It is an example of a peroxide-containing compound, which can be potentially reactive and may require special handling due to its peroxide nature.

74658-74-5

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74658-74-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74658-74-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,6,5 and 8 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 74658-74:
(7*7)+(6*4)+(5*6)+(4*5)+(3*8)+(2*7)+(1*4)=165
165 % 10 = 5
So 74658-74-5 is a valid CAS Registry Number.

74658-74-5Relevant academic research and scientific papers

Olefin Epoxidation with α-Substituted Hydroperoxides

Rebek, J.,McCready, R.

, p. 5602 - 5605 (2007/10/02)

A number of α-substituted hydroperoxides were examined for their ability to epoxidize olefins in a stereospecific manner.Hydroperoxy ethers, amines, carbonyl compounds, and nitriles showed this capability.Intramolecular epoxidation was demonstrated in cases where ortho esters of some olefinic alcohols were treated with H2O2, and methyl orthooleate - H2O2 mixtures also epoxidized the internal olefin in an intramolecular reaction.Attempts to generate chiral hydroperoxides for asymmetric epoxidation are described and structural features required for epoxidation reagents are discussed.

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