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The chemical compound "C12H8Cl2O2S2" is a complex organic molecule with a molecular formula indicating the presence of 12 carbon atoms, 8 hydrogen atoms, 2 chlorine atoms, 2 oxygen atoms, and 2 sulfur atoms. C12H8Cl2O2S2 likely has a structure that incorporates these elements in a way that could be associated with various functional groups, such as aromatic rings, halogenated substituents, and possibly sulfide or sulfate moieties. The specific arrangement of these atoms and the types of bonds they form would determine the compound's physical and chemical properties, such as its reactivity, solubility, and potential applications in fields like pharmaceuticals, agrochemicals, or materials science. Without additional structural information, it's challenging to provide a more detailed summary, but the molecular formula suggests a diverse range of possible chemical behaviors and uses.

2901-91-9

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2901-91-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2901-91-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,0 and 1 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2901-91:
(6*2)+(5*9)+(4*0)+(3*1)+(2*9)+(1*1)=79
79 % 10 = 9
So 2901-91-9 is a valid CAS Registry Number.

2901-91-9Downstream Products

2901-91-9Relevant academic research and scientific papers

A Kinetic-Electron Spin Resonance Study of the Self-reactions of Some Aromatic and Aliphatic Sulphonyl Radicals and Aromatic Sulphinyl Radicals

Bennett, John E.,Brunton, George,Gilbert, Bruce C.,Whittall, Peter E.

, p. 1359 - 1364 (2007/10/02)

A variety of aromatic and aliphatic sulphonyl radicals (RSO2.) have been found to undergo diffusion-controlled self-reaction in solution (with 2kt typically ca. 109 dm3 mol-1 s-1); reaction proceeds somewhat slower for some sterically hindered arenesulphonyl radicals (ArSO2.) and for some arenesulphinyl analogues (ArSO.).The observation of curved Arrhenius plots for some ArSO2. radicals, as well as the detection of ArSO. from sulphonyl precursors under steady-state conditions, is attributed to the thermal decomposition of an unstable intermediate formed by dimerisation (sulphur-to-oxygen) of ArSO2..A thermodynamic and kinetic analysis is presented.

FACILE REDUCTION OF SULFINIC ACID TO DISULFIDE WITH THIOL AND CHLOROTRIMETHYLSILANE

Oae, Shigeru,Togo, Hideo,Numata, Tatsuo,Fujimori, Ken

, p. 1193 - 1196 (2007/10/02)

Sulfinic acids were found to be readily reduced to the corresponding disulfide quantitatively at room temperature upon treatment with a mixture of thiols and chlorotrimethylsilane.

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