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bis<2-(N-dodecylcarboxamido)phenyl> diselenide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

124393-08-4

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124393-08-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 124393-08-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,3,9 and 3 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 124393-08:
(8*1)+(7*2)+(6*4)+(5*3)+(4*9)+(3*3)+(2*0)+(1*8)=114
114 % 10 = 4
So 124393-08-4 is a valid CAS Registry Number.

124393-08-4Downstream Products

124393-08-4Relevant academic research and scientific papers

Aromatic and Azaaromatic Diselenides, Benzisoselenazolones and Related Compounds as Immunomodulators Active in Humans: Synthesis and Properties

Mlochowski, Jacek,Kloc, Krystian,Syper, Ludwik,Inglot, Anna D.,Piasecki, Egbert

, p. 1239 - 1244 (2007/10/02)

Convenient syntheses of aryl diselenides 2, 1,2-benzisoselenazol-3(2H)-ones 4 and their 1-oxides 7 are reported.Reductive conversions of these compounds to bis(2-carbamoyl)phenyl diselenides 5 and oxidative cyclization of 5 to 1,2-benzisoselenazol-3(2H)-one 1-oxides 7 as the methods for the synthesis of these compounds are reported.Their ability to induce cytokines, such as TNF and IFN-γ, in human peripheral blood leucocyte cultures is described. - Key Words: 1,2-benzisoselenazol-3(2H)-ones/ Cytokine inducers/ Diselenides/ Interferon-gamma/ Tumor necrosis factor

Diselenobis-benzoic acid amides of primary and secondary amines and processes for the treatment of diseases in humans caused by a cell injury

-

, (2008/06/13)

The present invention relates to new diselenobis-benzoic acid amides of primary and secondary amines of the general formula (I): STR1 and processes for the treatment of diseases in humans caused by a cell injury.

LITHIUM DISELENIDE IN APROTIC MEDIUM - A CONVENIENT REAGENT FOR SYNTHESIS OF ORGANIC DISELENIDES

Syper, Ludwik,Mlochowski, Jacek

, p. 6119 - 6130 (2007/10/02)

The reduction of selenium with lithium in THF in the presence of diphenylacetylene as a catalyst afforded lithium diselenide, which reacted with electrophiles giving alkyl or aryl diselenides 1 - 3 and selenides 4, as by-products.The useful method for preparation of diselenides based on this reaction was elaborated.

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