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32636-05-8

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32636-05-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 32636-05-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,6,3 and 6 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 32636-05:
(7*3)+(6*2)+(5*6)+(4*3)+(3*6)+(2*0)+(1*5)=98
98 % 10 = 8
So 32636-05-8 is a valid CAS Registry Number.

32636-05-8Relevant academic research and scientific papers

BIARYL AND BIHETEROARYL COMPOUNDS USEFUL IN TREATING IRON DISORDERS

-

, (2008/12/07)

This invention is directed to compounds of formula (I): wherein m, n, R1, R2 and R3 are as defined herein, as a stereoisomer, enantiomer, tautomer thereof or mixtures thereof; or a pharmaceutically acceptable salt, solvate or prodrug thereof, for the treatment of iron disorders. This invention is also directed to pharmaceutical compositions comprising the compounds and methods of using the compounds to treat iron disorders.

Role of sulfide radical cations in electron transfer promoted molecular oxygenations at sulfur

Clennan, Edward L.,Liao, Chen

, p. 4057 - 4068 (2008/12/20)

The methylene blue, N-methylquinolinium tetrafluoroborate, and pyrylium-cation-sensitized photooxygenations of 5H, 7H-dibenzo[b,g] [1,5]dithiocin, 1, and 1,5-dithiacyclooctane, 2, have been investigated. The methylene blue sensitized reactions exhibit all of the characteristics of a singlet oxygen reaction including isotope effects for the formation of a hydroperoxysulfonium ylide and the ability of 1 and 2 to quench the time-resolved emission of singlet oxygen at 1270 nm. The product compositions in the N-methylquinolinium tetrafluoroborate and pyrylium-cation-sensitized reactions are dramatically different and are both different from that anticipated for the participation of singlet oxygen. This argues for different reaction mechanisms for all three sensitizers. However, both the quinolinium and pyrylium-cation-sensitized reactions display all of the characteristics of electron-transfer-initiated photooxygenations. Both sensitizers were quenched at nearly diffusion-limited rates by 1 and 2. Laser flash photolysis of mixtures of either sensitizer and 1 or 2 resulted in direct observation of the reduced sensitizer and the sulfide radical cation. In addition, electron-transfer reactions involving both sensitizers were shown to be exergonic. These results are consistent with the previously proposed outer sphere electron-transfer mechanism for N-methylquinolinium tetrafluoroborate and were used to argue for a new inner sphere mechanism for the pyrylium cation reactions.

Synthesis and Properties of Achiral Coronands Incorporating the Sulfide and Sulfoxide Functionality

Raguse, Burkhard,Ridley, Damon D.

, p. 1943 - 1952 (2007/10/02)

A number of polyether coronands incorporating sulfide and sulfoxide functionality and five or six ether oxygen atoms were prepared, their formation of complexes with alkali metal and ammonium salts were studied and the results were compared with analogous

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