Bis(2-bromoethyl) ether, 95%, Thermo Scientific Chemicals
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Thermo Scientific Chemicals
Bis(2-bromoethyl) ether, 95%, Thermo Scientific Chemicals
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25 g
5 g
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Catalog number L11510.14
also known as L11510-14
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25 g
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Chemical Identifiers
CAS5414-19-7
IUPAC Name1-bromo-2-(2-bromoethoxy)ethane
Molecular FormulaC4H8Br2O
InChI KeyFOZVXADQAHVUSV-UHFFFAOYSA-N
SMILESBrCCOCCBr
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SpecificationsSpecification SheetSpecification Sheet
FormLiquid
Refractive Index1.5110-1.5170 @ 20?C
Identification (FTIR)Conforms
Appearance (Color)Clear colorless to yellow to brown
Assay (GC)≥94.0%
Bis(2-bromoethyl) ether is used dfor synthesis of heterocyclic and crown ether. It is also used as a pharmaceutical intermediate.

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
Bis(2-bromoethyl) ether is used dfor synthesis of heterocyclic and crown ether. It is also used as a pharmaceutical intermediate.

Solubility
Not miscible or difficult to mix with water.

Notes
Keep container tightly sealed. Store in cool, dry conditions in well sealed containers. Incompatible with oxidizing agents and bases.
RUO – Research Use Only

General References:

  1. William A. Nugent. An Amino Alcohol Ligand for Highly Enantioselective Addition of Organozinc Reagents to Aldehydes: Serendipity Rules. Org. Lett. 2002, 4 (13 ), 2133-2136.
  2. Dieter Sellmann.; Herbert Kunstmann.; Falk Knoch.; Matthias Moll. Transition-metal complexes with sulfur ligands. Part 37. Iron, molybdenum, and ruthenium complexes with pentadentate OS4 and NHS4 ligands combining thiolato, thioether, and ether or amine donor functions: synthesis, structures, and reactivity of carbon monoxide, nitric oxide, trimethylphosphine and hydrazine derivatives. Inorg. Chem. 1988, 27 (23), 4183-4190.