Atomfair (8-Bromoquinolin-4-yl)methanol C10H8BrNO

Description (8-Bromoquinolin-4-yl)methanol (CAS No. 1190315-99-1) is a high-purity brominated quinoline derivative with the molecular formula C10H8BrNO . This compound is a versatile intermediate in organic synthesis and pharmaceutical research, featuring a reactive bromine substituent at the 8-position and a hydroxymethyl group at the 4-position of the quinoline scaffold. Its well-defined structure (IUPAC name: (8-bromoquinolin-4-yl)methanol) makes it valuable for metal-catalyzed cross-coupling reactions, nucleophilic substitutions, and as a precursor for fluorescent probes or bioactive molecules. Supplied as an off-white to light yellow crystalline powder with ??95% purity (HPLC), it is packaged under inert gas to ensure stability. Suitable for research use only…

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Description

Description

(8-Bromoquinolin-4-yl)methanol (CAS No. 1190315-99-1) is a high-purity brominated quinoline derivative with the molecular formula C10H8BrNO. This compound is a versatile intermediate in organic synthesis and pharmaceutical research, featuring a reactive bromine substituent at the 8-position and a hydroxymethyl group at the 4-position of the quinoline scaffold. Its well-defined structure (IUPAC name: (8-bromoquinolin-4-yl)methanol) makes it valuable for metal-catalyzed cross-coupling reactions, nucleophilic substitutions, and as a precursor for fluorescent probes or bioactive molecules. Supplied as an off-white to light yellow crystalline powder with ??95% purity (HPLC), it is packaged under inert gas to ensure stability. Suitable for research use only (RUO) in medicinal chemistry, materials science, and coordination chemistry applications.

  • CAS No: 1190315-99-1
  • Molecular Formula: C10H8BrNO
  • Molecular Weight: 238.08
  • Exact Mass: 236.97893
  • Monoisotopic Mass: 236.97893
  • IUPAC Name: (8-bromoquinolin-4-yl)methanol
  • SMILES: C1=CC2=C(C=CN=C2C(=C1)Br)CO
  • Synonyms: (8-bromoquinolin-4-yl)methanol, 1190315-99-1, 4-Quinolinemethanol, 8-bromo-, MFCD12828255, DTXSID40676541

Application

(8-Bromoquinolin-4-yl)methanol serves as a key building block in the synthesis of quinoline-based pharmaceuticals and agrochemicals. Researchers utilize its bromine moiety for Suzuki-Miyaura or Buchwald-Hartwig couplings to create complex heterocyclic systems. The hydroxymethyl group enables further derivatization into esters, ethers, or carbamates for drug discovery programs. It is also investigated as a potential ligand for transition metal catalysts in asymmetric synthesis.

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