meso-1,2-Dibromo-1,2-diphenylethane experience electrochemical dehalogenation in acetonitrile. The is reduced by electrogenerated C60−3.

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meso-1,2-Dibromo-1,2-diphenylethane(meso-SBr2) was used to study the reaction of ± and meso-SBr2 with 9-substituted fluorenide ion in dimethyl sulfoxide.

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If accessible for a offered product, the recommended re-test day or the expiration date can be uncovered on the Certificate the Analysis.

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Is Stilbene dibromide, Product 106550, optically active?

Generally, chiral molecules are optically active, rotating polarized light. Meso compounds, such as 106550, are unique in the there room chiral carbons in the molecule yet they are not optically active. Meso-1,2-Dibromo-1,2-diphenylethane has actually chiral carbons that space virtually identical however the plan of the teams on this carbon room different; the an outcome of this opposing results is a network optical rotation of zero.

In what solvents is Stilbene dibromide, Product 106550, soluble?

Sigma-Aldrich go not at this time test this product for solubility in a certain solvent. However, our quality regulate does solubilize this product with acetonitrile (with sonication) for analysis by HPLC at a concentration that 0.5mg/mL.

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Where have the right to I discover product comparable to meso-1,2-Dibromo-1,2-diphenylethane offered by Sigma-Aldrich?

The Sigma-Aldrich website provides numerous resources for locating assets with comparable structural characteristics. In ~ the bottom that the product info page because that product 106550, over there are links to "Related Categories." this links including listings the Sigma-Aldrich products that autumn in the same category as meso-1,2-Dibromo-1,2-diphenylethane. Alternatively, Sigma-Aldrich uses an online brochure that offers organized listings that products valuable for chemical synthesis, grouped by similar characteristics.

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Transportation information can be uncovered in section 14 the the product"s (M)SDS.To access the shipping info for this material, usage the connect on the product information page for the product. 

Debromination that meso-and (?)-1, 2-Dibromo-1, 2-diphenylethane by 9-Substituted Fluorenide Ions: Correlation in between Stereochemical Results and also Redox Potentials.
Electro-organic chemistry the fullerenes. Component 1. Indirect cathodic reduction of vic-dihalides and also perfluoroalkyl halides utilizing C60 as mediator. Cyclic voltammetric study and preparative-scale electrolysis.
Reduction the Vicinal Dihalides. I. The Electrochemical reduction of meso and also (?)-1, 2-Dibromo-1, 2-diphenylethane.