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Atomfair 2-Amino-5-bromo-4,6-dimethylpyrimidine C6H8BrN3

Description 2-Amino-5-bromo-4,6-dimethylpyrimidine (CAS No. 4214-57-7) is a high-purity brominated pyrimidine derivative with the molecular formula C6H8BrN3. This compound is a valuable heterocyclic building block for pharmaceutical and agrochemical research, featuring a reactive bromine substituent at the 5-position and an amino group at the 2-position of the pyrimidine ring. Its crystalline form and defined structure (IUPAC name: 5-bromo-4,6-dimethylpyrimidin-2-amine ) make it ideal for nucleophilic substitution reactions, Suzuki couplings, and other cross-coupling methodologies. Supplied with comprehensive analytical data including1H/13C NMR, HPLC, and mass spectrometry for quality assurance. Store under inert conditions at 2-8??C to maintain stability.

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Description

Description

2-Amino-5-bromo-4,6-dimethylpyrimidine (CAS No. 4214-57-7) is a high-purity brominated pyrimidine derivative with the molecular formula C6H8BrN3. This compound is a valuable heterocyclic building block for pharmaceutical and agrochemical research, featuring a reactive bromine substituent at the 5-position and an amino group at the 2-position of the pyrimidine ring. Its crystalline form and defined structure (IUPAC name: 5-bromo-4,6-dimethylpyrimidin-2-amine) make it ideal for nucleophilic substitution reactions, Suzuki couplings, and other cross-coupling methodologies. Supplied with comprehensive analytical data including 1H/13C NMR, HPLC, and mass spectrometry for quality assurance. Store under inert conditions at 2-8??C to maintain stability.

  • CAS No: 4214-57-7
  • Molecular Formula: C6H8BrN3
  • Molecular Weight: 202.05
  • Exact Mass: 200.99016
  • Monoisotopic Mass: 200.99016
  • IUPAC Name: 5-bromo-4,6-dimethylpyrimidin-2-amine
  • SMILES: CC1=C(C(=NC(=N1)N)C)Br
  • Synonyms: 2-Amino-5-bromo-4,6-dimethylpyrimidine, 4214-57-7, DTXSID50372229, DTXCID60323262, 661-921-7

Application

This compound serves as a key intermediate in the synthesis of nucleoside analogs and kinase inhibitors, particularly in antiviral and anticancer drug discovery. Its bromine moiety enables facile functionalization via metal-catalyzed cross-coupling reactions for library synthesis. Researchers also utilize it as a precursor for fluorescent dyes and coordination complexes in materials science. The dimethyl substitution pattern enhances metabolic stability in medicinal chemistry applications.

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