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Atomfair 3-Bromo-5H-benzofuro[3,2-c]carbazole C18H10BrNO

Description 3-Bromo-5H-benzofuro[3,2-c]carbazole (CAS No. 1373227-29-2) is a high-purity heterocyclic organic compound with the molecular formula C18H10BrNO. This brominated benzofurocarbazole derivative is a valuable building block for pharmaceutical research, material science, and organic synthesis. Its rigid polycyclic structure and bromine substituent make it an ideal intermediate for Suzuki coupling, Buchwald-Hartwig amination, and other cross-coupling reactions. The compound is supplied as a stable solid with ??95% purity (HPLC), ensuring reproducibility in advanced research applications. Proper storage under inert conditions is recommended to maintain its integrity.

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Description

Description

3-Bromo-5H-benzofuro[3,2-c]carbazole (CAS No. 1373227-29-2) is a high-purity heterocyclic organic compound with the molecular formula C18H10BrNO. This brominated benzofurocarbazole derivative is a valuable building block for pharmaceutical research, material science, and organic synthesis. Its rigid polycyclic structure and bromine substituent make it an ideal intermediate for Suzuki coupling, Buchwald-Hartwig amination, and other cross-coupling reactions. The compound is supplied as a stable solid with ??95% purity (HPLC), ensuring reproducibility in advanced research applications. Proper storage under inert conditions is recommended to maintain its integrity.

  • CAS No: 1373227-29-2
  • Molecular Formula: C18H10BrNO
  • Molecular Weight: 336.2
  • Exact Mass: 334.99458
  • Monoisotopic Mass: 334.99458
  • IUPAC Name: 3-bromo-5H-[1]benzofuro[3,2-c]carbazole
  • SMILES: C1=CC=C2C(=C1)C3=C(O2)C4=C(C=C3)NC5=C4C=CC(=C5)Br
  • Synonyms: 3-Bromo-5H-benzofuro[3,2-c]carbazole, 1373227-29-2, SCHEMBL14992666

Application

3-Bromo-5H-benzofuro[3,2-c]carbazole serves as a key precursor in the synthesis of novel carbazole-based OLED materials due to its electron-rich aromatic system. Researchers utilize this compound to develop pharmacologically active molecules targeting kinase inhibition and anticancer therapies. Its bromine functionality allows for further derivatization in Pd-catalyzed cross-coupling reactions to construct complex heterocyclic architectures.

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