Atomfair 5-Bromonaphthalen-1-amine C10H8BrN

Description 5-Bromonaphthalen-1-amine (CAS No. 4766-33-0) is a high-purity brominated naphthylamine compound with the molecular formula C10H8BrN . This aromatic amine is a versatile intermediate in organic synthesis, particularly in the preparation of dyes, pharmaceuticals, and advanced materials. Its unique structure, featuring a bromine substituent at the 5-position and an amine group at the 1-position of the naphthalene ring, enables selective functionalization for complex molecular architectures. Our product is rigorously tested for purity (typically ??98% by HPLC) and is supplied as a crystalline solid with excellent batch-to-batch consistency. Ideal for researchers developing fluorescent probes, liquid crystals, or bioactive compounds due to…

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Description

Description

5-Bromonaphthalen-1-amine (CAS No. 4766-33-0) is a high-purity brominated naphthylamine compound with the molecular formula C10H8BrN. This aromatic amine is a versatile intermediate in organic synthesis, particularly in the preparation of dyes, pharmaceuticals, and advanced materials. Its unique structure, featuring a bromine substituent at the 5-position and an amine group at the 1-position of the naphthalene ring, enables selective functionalization for complex molecular architectures. Our product is rigorously tested for purity (typically ??98% by HPLC) and is supplied as a crystalline solid with excellent batch-to-batch consistency. Ideal for researchers developing fluorescent probes, liquid crystals, or bioactive compounds due to its electron-rich aromatic system and halogen reactivity.

  • CAS No: 4766-33-0
  • Molecular Formula: C10H8BrN
  • Molecular Weight: 222.08
  • Exact Mass: 220.98401
  • Monoisotopic Mass: 220.98401
  • IUPAC Name: 5-bromonaphthalen-1-amine
  • SMILES: C1=CC2=C(C=CC=C2Br)C(=C1)N
  • Synonyms: 5-bromonaphthalen-1-amine, 4766-33-0, DTXSID90597676, DTXCID40548436, 676-034-0

Application

5-Bromonaphthalen-1-amine serves as a key building block in the synthesis of organic semiconductors and optoelectronic materials. It is employed in the preparation of Schiff base ligands for transition metal catalysis and as a precursor for brominated azo dyes. Researchers utilize this compound in medicinal chemistry for the development of kinase inhibitors and other pharmacologically active naphthalene derivatives.

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