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Atomfair Bromomethyl methyl ether C2H5BrO

Description Bromomethyl methyl ether (CAS No. 26978-64-3), also known as bromo(methoxy)methane, is a highly reactive alkylating agent with the molecular formula C2H5BrO. This organobromine compound is widely utilized in organic synthesis, particularly in the introduction of methoxymethyl groups. Its clear to pale yellow liquid form and pungent odor make it easily identifiable in laboratory settings. With a molecular weight of 124.97 g/mol, this reagent is commonly employed in nucleophilic substitution reactions and as a protecting group intermediate. Due to its hazardous nature, it should be handled with extreme caution under controlled conditions. Proper storage in a cool, dry, and well-ventilated…

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Description

Description

Bromomethyl methyl ether (CAS No. 26978-64-3), also known as bromo(methoxy)methane, is a highly reactive alkylating agent with the molecular formula C2H5BrO. This organobromine compound is widely utilized in organic synthesis, particularly in the introduction of methoxymethyl groups. Its clear to pale yellow liquid form and pungent odor make it easily identifiable in laboratory settings. With a molecular weight of 124.97 g/mol, this reagent is commonly employed in nucleophilic substitution reactions and as a protecting group intermediate. Due to its hazardous nature, it should be handled with extreme caution under controlled conditions. Proper storage in a cool, dry, and well-ventilated area is essential to maintain stability.

  • CAS No: 26978-64-3
  • Molecular Formula: C2H5BrO
  • Molecular Weight: 124.96
  • Exact Mass: 123.95238
  • Monoisotopic Mass: 123.95238
  • IUPAC Name: bromo(methoxy)methane
  • SMILES: COCBr
  • Synonyms: Bromomethyl methyl ether, Methane, bromomethoxy-, Bromo(methoxy)methane, Methoxymethyl bromide, Ether, bromomethyl methyl

Application

Bromomethyl methyl ether serves as a versatile reagent in organic synthesis, primarily used for methoxymethylation reactions. It is particularly valuable in the protection of hydroxyl groups during multi-step synthetic processes. The compound finds application in pharmaceutical intermediates and fine chemical production. Researchers also utilize it in polymer chemistry for modifying functional groups. Its reactivity makes it suitable for creating complex molecular architectures in medicinal chemistry.

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