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meso-1,2-Dibromo-1,2-diphenylethane, 97%, Thermo Scientific Chemicals
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Catalog number L04956.14
also known as L04956-14
Price (USD)/ Each
145.00
-
Quantity:
25 g
Price (USD)/ Each
145.00
meso-1,2-Dibromo-1,2-diphenylethane, 97%, Thermo Scientific Chemicals
Catalog numberL04956.14
Price (USD)/ Each
145.00
-
Chemical Identifiers
CAS13440-24-9
IUPAC Name(1,2-dibromo-2-phenylethyl)benzene
Molecular FormulaC14H12Br2
InChI KeyGKESIQQTGWVOLH-UHFFFAOYNA-N
SMILESBrC(C(Br)C1=CC=CC=C1)C1=CC=CC=C1
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Specifications
Specification Sheet
Specification SheetFormCrystals or powder or crystalline powder
Assay (HPLC)≥96.0%
Identification (FTIR)Conforms
Appearance (Color)White to pale cream
meso-1,2-Dibromo-1,2-diphenylethane is used to study the reaction of ± and meso-SBr2 with 9-substituted fluorenide ions in dimethyl sulfoxide. It undergoes electrochemical dehalogenation in acetonitrile.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
meso-1,2-Dibromo-1,2-diphenylethane is used to study the reaction of ± and meso-SBr2 with 9-substituted fluorenide ions in dimethyl sulfoxide. It undergoes electrochemical dehalogenation in acetonitrile.
Solubility
Insoluble in water.
Notes
Incompatible materials are Strong oxidizing agents. Store in cool place. Keep container tightly closed in a dry and well-ventilated place.
meso-1,2-Dibromo-1,2-diphenylethane is used to study the reaction of ± and meso-SBr2 with 9-substituted fluorenide ions in dimethyl sulfoxide. It undergoes electrochemical dehalogenation in acetonitrile.
Solubility
Insoluble in water.
Notes
Incompatible materials are Strong oxidizing agents. Store in cool place. Keep container tightly closed in a dry and well-ventilated place.
RUO – Research Use Only
General References:
- P Fawell; J Avraamides and G Hefter. Reduction of Vicinal Dihalides. I. The Electrochemical Reduction of meso and (±)-1,2-Dibromo-1,2-diphenylethane.Australian Journal of Chemistry.1990, 43 (8), 1421 - 1430.
- John E. Gordon; Victor S. K. Chang. Reduction of meso-1,2-dibromo-1,2-diphenylethane to 1,2-diphenylethane by hydrazine.J. Org. Chem.1973,38 (17), 3062-3064.