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Atomfair 1-Bromonaphthalene-2-carbaldehyde C11H7BrO

Description 1-Bromonaphthalene-2-carbaldehyde (CAS No. 3378-82-3) is a high-purity organic compound with the molecular formula C11H7BrO . This aromatic aldehyde is characterized by a bromine substituent at the 1-position and a formyl group at the 2-position of the naphthalene ring, making it a versatile intermediate in synthetic organic chemistry. It is supplied as a crystalline solid with a distinct aromatic odor, ensuring optimal reactivity for cross-coupling reactions, nucleophilic substitutions, and other advanced transformations. Ideal for researchers in pharmaceuticals, agrochemicals, and materials science, this compound is rigorously tested for purity (typically ??95% by GC or HPLC) and is packaged under inert conditions…

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Description

Description

1-Bromonaphthalene-2-carbaldehyde (CAS No. 3378-82-3) is a high-purity organic compound with the molecular formula C11H7BrO. This aromatic aldehyde is characterized by a bromine substituent at the 1-position and a formyl group at the 2-position of the naphthalene ring, making it a versatile intermediate in synthetic organic chemistry. It is supplied as a crystalline solid with a distinct aromatic odor, ensuring optimal reactivity for cross-coupling reactions, nucleophilic substitutions, and other advanced transformations. Ideal for researchers in pharmaceuticals, agrochemicals, and materials science, this compound is rigorously tested for purity (typically ??95% by GC or HPLC) and is packaged under inert conditions to ensure stability. Store in a cool, dry place away from light and moisture to maintain integrity.

  • CAS No: 3378-82-3
  • Molecular Formula: C11H7BrO
  • Molecular Weight: 235.08
  • Exact Mass: 233.96803
  • Monoisotopic Mass: 233.96803
  • IUPAC Name: 1-bromonaphthalene-2-carbaldehyde
  • SMILES: C1=CC=C2C(=C1)C=CC(=C2Br)C=O
  • Synonyms: 3378-82-3, 1-Bromonaphthalene-2-carbaldehyde, 1-bromo-2-naphthalenecarboxaldehyde, EINECS 222-180-1, DTXSID60187442

Application

1-Bromonaphthalene-2-carbaldehyde serves as a key building block in the synthesis of complex organic molecules, particularly in pharmaceutical research for developing bioactive compounds. It is widely used in Suzuki-Miyaura and other palladium-catalyzed cross-coupling reactions to construct polycyclic aromatic systems. Additionally, its aldehyde group enables further functionalization via condensation or reduction, making it valuable for creating dyes, ligands, and advanced materials.

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