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The chemical "5-CH3O-6-NO2-C6F4" is a complex organic molecule with a fluorinated benzene ring. It features a 4-fluorine substituted benzene ring, with a methyl group (CH3) attached to the 5th carbon and a nitro group (NO2) on the 6th carbon. 5-CH3O-6-NO2-C6F4 is likely to be a derivative of a fluorinated phenol, given the presence of the hydroxyl group (OH) indicated by "O-". The structure suggests potential applications in areas such as pharmaceuticals, agrochemicals, or materials science, where fluorinated compounds are valued for their unique properties. The specific arrangement of functional groups could influence its reactivity, stability, and potential interactions with biological systems or materials.

3152-99-6

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3152-99-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3152-99-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,5 and 2 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 3152-99:
(6*3)+(5*1)+(4*5)+(3*2)+(2*9)+(1*9)=76
76 % 10 = 6
So 3152-99-6 is a valid CAS Registry Number.

3152-99-6Relevant academic research and scientific papers

Mechanism of Oxidative Activation of Fluorinated Aromatic Compounds by N-Bridged Diiron-Phthalocyanine: What Determines the Reactivity?

Colomban, Cédric,Tobing, Anthonio H.,Mukherjee, Gourab,Sastri, Chivukula V.,Sorokin, Alexander B.,de Visser, Sam P.

supporting information, p. 14320 - 14331 (2019/11/03)

The biodegradation of compounds with C?F bonds is challenging due to the fact that these bonds are stronger than the C?H bond in methane. In this work, results on the unprecedented reactivity of a biomimetic model complex that contains an N-bridged diiron-phthalocyanine are presented; this model complex is shown to react with perfluorinated arenes under addition of H2O2 effectively. To get mechanistic insight into this unusual reactivity, detailed density functional theory calculations on the mechanism of C6F6 activation by an iron(IV)-oxo active species of the N-bridged diiron phthalocyanine system were performed. Our studies show that the reaction proceeds through a rate-determining electrophilic C?O addition reaction followed by a 1,2-fluoride shift to give the ketone product, which can further rearrange to the phenol. A thermochemical analysis shows that the weakest C?F bond is the aliphatic C?F bond in the ketone intermediate. The oxidative defluorination of perfluoroaromatics is demonstrated to proceed through a completely different mechanism compared to that of aromatic C?H hydroxylation by iron(IV)-oxo intermediates such as cytochrome P450 Compound I.

Constructing a catalytic cycle for c-f to c-x (x = o, s, n) bond transformation based on gold-mediated ligand nucleophilic attack

Hu, Ji-Yun,Zhang, Jing,Wang, Gao-Xiang,Sun, Hao-Ling,Zhang, Jun-Long

supporting information, p. 2274 - 2283 (2017/01/16)

A tricoordinated gold(I) chloride complex, tBuXantphosAuCl, supported by a sterically bulky 9,9-dimethyl-4,5-bis(di-Tert-butylphosphino)xanthene ligand (tBuXantphos) was synthesized. This complex features a remarkably longer Au?Cl bond length [2.632(1) ?] than bicoordinated linear gold complexes (2.27-2.30 ?) and tricoordinated XantphosAuCl [2.462(1) ?]. Single-crystal Xray diffraction analysis of a cocrystal of tBuXantphosAuCl and pentafluoronitrobenzene (PFNB) and UV-vis spectroscopic titration experiments revealed the existence of an anion-φ interaction between the Cl anion ligand and PFNB. Stoichiometric reaction between PFNB and tBuXantphosAuOtBu, after replacement of Cl by a more nucleophilic tBuO anion ligand, showed higher reactivity and para selectivity in the transformation of C-F to C-OtBu bond, distinctively different from that when only KOtBu was used (ortho selectivity) under the identical condition. Mechanistic studies including density functional theory calculations suggested a gold-mediated nucleophilic ligand attack of the C?F bond pathway via an SNAr process. On the basis of these results, using trimethylsilyl derivatives TMS-X (X = OMe, SEt, NEt) as the nucleophilic ligand source and the fluorine acceptor, catalytic transformation of the C-F bond of aromatic substrates to the C-X (X = O, S, N) bond was achieved with tBuXantphosAuCl as the catalyst (up to 20 turnover numbers).

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