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15446-31-8

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15446-31-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15446-31-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,4,4 and 6 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 15446-31:
(7*1)+(6*5)+(5*4)+(4*4)+(3*6)+(2*3)+(1*1)=98
98 % 10 = 8
So 15446-31-8 is a valid CAS Registry Number.

15446-31-8Relevant articles and documents

A tetranitrosyl [4Fe-4S] cluster forms en route to roussins black anion: Nitric oxide reactivity of [Fe4S4(LS3)L] 2-

Victor, Eric,Lippard, Stephen J.

, p. 5311 - 5320 (2014)

Previous studies provide evidence that [4Fe-4S] clusters serve as targets of reactive nitrogen oxide species in biology. The products of this reaction range from dinitrosyliron complexes, [Fe(NO)2L2] -, to Roussins black anion, [Fe4S3(NO) 7]-. To date, the pathways by which these reactions occur have not been fully elucidated. In this study, we prepared the site-differentiated complexes [Fe4S4(LS 3)L]2- (LS3 = 1,3,5-tris(4,6-dimethyl-3- mercaptophenylthio)-2,4,6-tris(p-tolylthio)benzene; L = Cl, SEt, SPh, N 3, 2-SPyr, Tp, S2CNEt2) to serve as synthetic models for biological [4Fe-4S] clusters and studied their reactivity toward NO(g) and Ph3CSNO. The products were characterized by X-ray crystallography, mass spectrometry, and IR, electron paramagnetic resonance (EPR), and 1H NMR spectroscopy. In all cases reported here, the reactions proceed via formation of the S = 1/2 species [Fe4S4(NO)4]-, which ultimately converts to EPR-silent [Fe4S3(NO)7] -.

Glutathione peroxidase mimics based on conformationally-restricted,peri-like, 4,5-disubstituted fluorene dichalcogenides

Capperucci, Antonella,Figliola, Carlotta,Grainger, Richard S.,Jagdev, Kesar,Lownes, Jack W.,Male, Louise,Tanini, Damiano

, p. 10565 - 10569 (2021/12/27)

Glutathione peroxidase (GPx) regulates cellular peroxide levels through glutathione oxidation. GPx-mimics based on 4,5-disubstituted fluorene diselenides, their oxides, and ditellurides show catalytic activities consistent with conformational restriction

Reactivity of [U(CH2SiMe2NSiMe3)(NR2)2] (R = SiMe3) with elemental chalcogens: Towards a better understanding of chalcogen atom transfer in the actinides

Smiles, Danil E.,Wu, Guang,Hayton, Trevor W.

supporting information, p. 7563 - 7566 (2015/10/12)

The reaction of the U(iv) metallacycle, [U(CH2SiMe2NSiMe3)(NR2)2] (R = SiMe3) with the elemental chalcogens, E (E = S, Se, Te) affords the insertion products, [U(ECH2SiMe2/

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