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CAS 63184-61-2

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3-(Bromomethyl)furan

Description:
3-(Bromomethyl)furan is an organic compound characterized by the presence of a furan ring substituted with a bromomethyl group at the 3-position. Its molecular structure features a five-membered aromatic ring containing one oxygen atom, which contributes to its reactivity and potential applications in organic synthesis. The bromomethyl group introduces a halogen, making the compound a useful intermediate in various chemical reactions, including nucleophilic substitutions and coupling reactions. This compound is typically a colorless to pale yellow liquid with a distinctive odor. It is soluble in organic solvents, which enhances its utility in synthetic chemistry. Due to the presence of the bromine atom, 3-(Bromomethyl)furan can participate in electrophilic aromatic substitution reactions, making it valuable for the synthesis of more complex molecules. Safety considerations are important when handling this compound, as brominated compounds can be hazardous. Proper storage and handling protocols should be followed to minimize exposure and ensure safe use in laboratory settings.
Formula:C5H5BrO
InChI:InChI=1/C5H5BrO/c6-3-5-1-2-7-4-5/h1-2,4H,3H2
SMILES:c1cocc1CBr
Synonyms:
  • Furan, 3-(Bromomethyl)-
  • 3-(Bromomethyl)furan
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Found 2 products.
  • 3-(Bromomethyl)furan 20% w/w solution in toluene
    Apollo Scientific
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    3-(Bromomethyl)furan 20% w/w solution in toluene

    CAS:
    3-(Bromomethyl)furan 20% w/w solution in toluene
    Formula:C5H5BrO
    Purity:≥95%
    Color and Shape: yellow liquid
    Molecular weight:161.00g/mol

    Ref: 54-OR400006

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  • 3-(Bromomethyl)furan
    Biosynth
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    3-(Bromomethyl)furan

    CAS:
    <p>3-(Bromomethyl)furan is a synthetic compound that is used in the synthesis of natural products and pharmaceuticals. The asymmetric synthesis of 3-(bromomethyl)furan was achieved through a cross-coupling reaction between propanediol and an organometallic reagent (tetronic acid). This reaction proceeds through a stereogenic spirocyclization, which involves the formation of two different stereoisomers. The use of 3-(bromomethyl)furan in the synthesis of lactams has been shown to be an effective way to produce antibacterial molecules. This process starts with nucleophilic attack at the c-3 position by an organometallic reagent, followed by desymmetrization to form a lactam.</p>
    Formula:C5H5BrO
    Purity:Min. 95%
    Molecular weight:161 g/mol

    Ref: 3D-FB148923

    25mg
    863.00€