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1073269-05-2

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1073269-05-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1073269-05-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,7,3,2,6 and 9 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1073269-05:
(9*1)+(8*0)+(7*7)+(6*3)+(5*2)+(4*6)+(3*9)+(2*0)+(1*5)=142
142 % 10 = 2
So 1073269-05-2 is a valid CAS Registry Number.

1073269-05-2Downstream Products

1073269-05-2Relevant academic research and scientific papers

Synthesis and structure - activity correlation studies of secondary- and tertiary-amine-based glutathione peroxidase mimics

Bhabak, Krishna P.,Mugesh, Govindasamy

body text, p. 9846 - 9854 (2010/04/29)

In this study, a series of secondary- and tertiary-amino-substituted diaryl diselenides were synthesized and studied for their glutathione peroxidase (GPx) like antioxidant activities with H2O2, cumene hydroperoxide, or tBuOOH as sub

A simple and efficient strategy to enhance the antioxidant activities of amino-substituted glutathione peroxidase mimics

Bhabak, Krishna P.,Mugesh, Govindasamy

body text, p. 8640 - 8651 (2009/10/24)

The glutathione peroxidase (GPx) activities of some diaryl diselenides incorporating tertiary amino groups were studied with H2O 2, Cum-OOH, and tBuOOH as substrates and with PhSH as thiol co-substrate. Simple replacement of a hydrogen atom with a methoxy group dramatically enhances the GPx activity. The introduction of methoxy substituents ortho to selenium in N,N-dialkylbenzylamine-based compounds makes the basicity of the amino groups perfect for the catalysis. The presence of 6-OMe groups prevents possible Se-N interactions in the selenols, increasing their zwitterionic characters. The methoxy substituents also protect the selenium in the selenenic acid intermediates from overoxidation to seleninic acids or irreversible inactivation to selenonic acid derivatives. The additional substituents also play a crucial role in the selenenyl sulfide intermediates, by preventing thiol exchange reactions-which would normally lead to an inactivation pathway-at the selenium centers. The strengths of Se...N interactions in the selenenyl sulfide intermediates are dra-matically reduced upon introduction of the methoxy substituents, which not only reduce the thiol exchange reactions at selenium but also enhance the nucleophilic attack of the incoming thiols at sulfur. The facile attack of thiols at sulfur in the selenenyl sulfides also prevents the reactions between the selenenyl sulfides and H2O2 that can regenerate the selenenic acids (reverseGPx cycle). These studies reveal that the simple 6-OMe groups play multiple roles in each of the catalytically active intermediates by introducing steric and electronic effects that are required for efficient catalysis.

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