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7,8-Dimethyl-3-(propane-1-sulfinyl)-10H-benzo[g]pteridine-2,4-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

36469-13-3

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36469-13-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 36469-13-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,4,6 and 9 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 36469-13:
(7*3)+(6*6)+(5*4)+(4*6)+(3*9)+(2*1)+(1*3)=133
133 % 10 = 3
So 36469-13-3 is a valid CAS Registry Number.

36469-13-3Upstream product

36469-13-3Downstream Products

36469-13-3Relevant academic research and scientific papers

On the Mechanism of Flavin-Catalyzed Dehydrogenation α,β to an Acyl Function. The Mechanism of 1,5-Dihydroflavin Reduction of Maleimides

Venkataram, U. V.,Bruice, Thomas C.

, p. 5703 - 5709 (1984)

The dihydroflavin reductions of maleimide (MI) and N-methylmaleimide (MMI) have been investigated using the water-soluble 1,5-dihydro-3-(3-sulfopropyl)lumiflavin (FlH2).The reaction of the dihydroflavin with MI and MMI to yield oxidized flavin (Flox) and succinimides is biphasic.The first phase involves general-acid-assisted nucleophilic attack of dihydroflavin anion (FlH-) upon the maleimide to yield 4α-substituted 4a,5-dihydroflavin covalent adducts.The Broensted α for the general-acid catalysis is -0.1 to -0.2.This observation would be expected for a Michael addition to FlH- upon MMI to yield an unstable anionic 4a adduct which is trapped by proton transfer from general-acid species.The rate of decomposition of the intermediate to yield Flox and succinimide is not measurably dependent upon the concentration of the general-base species.The reaction was found to be first order in ->.A mechanism involving preequilibrium ionization of the N(5)-H followed by elimination of succinimide anion (specific-base catalysis) and formation of Flox would require that the pKa for dissociation of the aniline-like N(5)-H is less than 23 in order that the rate of elimination from the anion does not exceed that for the vibration of the C-C bond that is broken.It is concluded that the HO--catalyzed elimination represents a concerted process with a Broensted β approaching 1.0.From the results of this study and by involving the principal of microscopic reversibility the mechanism of N-methylsuccinimide anion oxidation by Flox to yield maleimide and FlH- can be constructed.The possible implications of this mechanism to the mechanism of such dehydrogenating flavoenzymes as succinic acid dehydrogenase, fumarate reductase, acyl-CoA dehydrogenase , and acyl-CoA dehydrogenase, and acyl-CoA oxidase are considered.

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