5414-19-7 | 1-Bromo-2-(2-bromoethoxy)ethane

Availability
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Description

• Catalog Number: AB59576
• Chemical Name: 1-Bromo-2-(2-bromoethoxy)ethane
• CAS Number: 5414-19-7
• Molecular Formula: C4H8Br2O
• Molecular Weight: 231.9137
• MDL Number: MFCD00039196
• SMILES: BrCCOCCBr
• NSC Number: 8025

Computed Properties

• Complexity: 28.9
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 7
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 4
• XLogP3: 1.6

Upstream Synthesis Route

1-Bromo-2-(2-bromoethoxy)ethane, also known as $name$, is a versatile chemical compound widely used in chemical synthesis. Its unique structure allows for various applications in organic reactions, making it a valuable reagent in the laboratory and industrial settings.One key application of this compound is its role as a building block in the synthesis of complex organic molecules. By serving as a halogenated intermediate, $name$ can participate in a range of substitution reactions to form new carbon-carbon or carbon-heteroatom bonds. This versatility makes it particularly useful in the preparation of pharmaceuticals, agrochemicals, and fine chemicals.Additionally, $name$ can act as a reagent in cross-coupling reactions, where it undergoes coupling with other organic compounds under appropriate conditions to generate more intricate structures. This ability to form diverse chemical bonds makes it an essential tool for chemists seeking to design and produce novel compounds with specific properties.Furthermore, the presence of two bromine atoms in $name$ enhances its reactivity in certain processes, such as radical reactions and halogenation reactions. This dual functionality opens up opportunities for selective transformations and allows for the introduction of bromine-containing moieties into target molecules.In summary, 1-Bromo-2-(2-bromoethoxy)ethane is a valuable compound in chemical synthesis, offering a wide range of applications in the creation of complex organic molecules. Its versatile reactivity and unique structure make it a valuable tool for synthetic chemists aiming to develop new materials and compounds with tailored properties.

Literature

• An amino alcohol ligand for highly enantioselective addition of organozinc reagents to aldehydes: serendipity rules.

  Organic letters 20020627