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Atomfair 5,8-Dimethoxy-[1,2,4]triazolo[1,5-c]pyrimidin-2-amine C7H9N5O2

Description 5,8-Dimethoxy-[1,2,4]triazolo[1,5-c]pyrimidin-2-amine (CAS No. 219715-62-5) is a high-purity heterocyclic compound with the molecular formula C7H9N5O2. This specialized chemical features a triazolopyrimidine core substituted with dimethoxy and amine functional groups, making it a valuable intermediate for pharmaceutical and agrochemical research. With a molecular weight of 195.18 g/mol , it is supplied as a crystalline solid with ??95% purity (HPLC). Ideal for medicinal chemistry applications, this compound is particularly useful in the development of kinase inhibitors and other biologically active molecules. Proper storage at 2-8??C in a tightly sealed container is recommended to ensure long-term stability.

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Description

Description

5,8-Dimethoxy-[1,2,4]triazolo[1,5-c]pyrimidin-2-amine (CAS No. 219715-62-5) is a high-purity heterocyclic compound with the molecular formula C7H9N5O2. This specialized chemical features a triazolopyrimidine core substituted with dimethoxy and amine functional groups, making it a valuable intermediate for pharmaceutical and agrochemical research. With a molecular weight of 195.18 g/mol, it is supplied as a crystalline solid with ??95% purity (HPLC). Ideal for medicinal chemistry applications, this compound is particularly useful in the development of kinase inhibitors and other biologically active molecules. Proper storage at 2-8??C in a tightly sealed container is recommended to ensure long-term stability.

  • CAS No: 219715-62-5
  • Molecular Formula: C7H9N5O2
  • Molecular Weight: 195.18
  • Exact Mass: 195.07562455
  • Monoisotopic Mass: 195.07562455
  • IUPAC Name: 5,8-dimethoxy-[1,2,4]triazolo[1,5-c]pyrimidin-2-amine
  • SMILES: COC1=CN=C(N2C1=NC(=N2)N)OC
  • Synonyms: 5,8-Dimethoxy-[1,2,4]triazolo[1,5-c]pyrimidin-2-amine, DTXSID70466114, 5,8-dimethoxy-(1,2,4)triazolo(1,5-c)pyrimidin-2-amine, DTXCID30416933, 875-177-8

Application

This compound serves as a key building block in medicinal chemistry for the synthesis of triazolopyrimidine-based drug candidates. Researchers utilize it in the development of potential kinase inhibitors targeting various disease pathways. The dimethoxy and amine substitutions make it particularly valuable for structure-activity relationship studies in anticancer and antimicrobial research. Its unique heterocyclic structure also finds applications in agrochemical research for novel pesticide development.

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