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Atomfair Methyl 4-(2-bromoethynyl)benzoate C10H7BrO2

Description Methyl 4-(2-bromoethynyl)benzoate (CAS No. 225928-10-9) is a high-purity organic compound with the molecular formula C10H7BrO2, widely utilized in synthetic organic chemistry and pharmaceutical research. This compound features a reactive bromoethynyl group attached to a benzoate ester, making it a versatile building block for cross-coupling reactions, such as Sonogashira and Suzuki couplings. Its crystalline form ensures consistent reactivity, and it is supplied with detailed analytical certifications (including1H NMR,13C NMR, and HPLC) to guarantee quality. Ideal for researchers developing novel heterocycles, conjugated polymers, or bioactive molecules. Store under inert conditions at recommended temperatures to maintain stability.

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Description

Description

Methyl 4-(2-bromoethynyl)benzoate (CAS No. 225928-10-9) is a high-purity organic compound with the molecular formula C10H7BrO2, widely utilized in synthetic organic chemistry and pharmaceutical research. This compound features a reactive bromoethynyl group attached to a benzoate ester, making it a versatile building block for cross-coupling reactions, such as Sonogashira and Suzuki couplings. Its crystalline form ensures consistent reactivity, and it is supplied with detailed analytical certifications (including 1H NMR, 13C NMR, and HPLC) to guarantee quality. Ideal for researchers developing novel heterocycles, conjugated polymers, or bioactive molecules. Store under inert conditions at recommended temperatures to maintain stability.

  • CAS No: 225928-10-9
  • Molecular Formula: C10H7BrO2
  • Molecular Weight: 239.06
  • Exact Mass: 237.96294
  • Monoisotopic Mass: 237.96294
  • IUPAC Name: methyl 4-(2-bromoethynyl)benzoate
  • SMILES: COC(=O)C1=CC=C(C=C1)C#CBr
  • Synonyms: Methyl 4-(2-bromoethynyl)benzoate, 895-853-6, methyl 4-(bromoethynyl)benzoate, 225928-10-9, MFCD16251110

Application

Methyl 4-(2-bromoethynyl)benzoate serves as a key intermediate in the synthesis of advanced materials and pharmaceuticals. It is employed in palladium-catalyzed coupling reactions to construct conjugated systems for organic electronics. Researchers also use it to introduce ethynyl-benzoate motifs into drug candidates for enhanced binding properties. Its bromoethynyl group enables facile functionalization in peptide and small-molecule derivatization.

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