Cas no 852921-87-0 (4-(2-methoxyethoxy)pyrimidin-2-amine)

4-(2-methoxyethoxy)pyrimidin-2-amine structure
852921-87-0 structure
Product Name:4-(2-methoxyethoxy)pyrimidin-2-amine
CAS No:852921-87-0
MF:C7H11N3O2
MW:169.181141138077
MDL:MFCD17013097
CID:4236452
PubChem ID:79001937
Update Time:2025-07-19

4-(2-methoxyethoxy)pyrimidin-2-amine Chemical and Physical Properties

Names and Identifiers

    • 2-Pyrimidinamine, 4-(2-methoxyethoxy)-
    • 4-(2-methoxyethoxy)pyrimidin-2-amine
    • 4-(2-Methoxyethoxy)-2-pyrimidinamine
    • 852921-87-0
    • EN300-207888
    • CJB92187
    • Z1255437598
    • AKOS017514949
    • DB-183839
    • MDL: MFCD17013097
    • Inchi: 1S/C7H11N3O2/c1-11-4-5-12-6-2-3-9-7(8)10-6/h2-3H,4-5H2,1H3,(H2,8,9,10)
    • InChI Key: AAUDKFQCBFLDCE-UHFFFAOYSA-N
    • SMILES: C1(N)=NC=CC(OCCOC)=N1

Computed Properties

  • Exact Mass: 169.085126602Da
  • Monoisotopic Mass: 169.085126602Da
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 5
  • Heavy Atom Count: 12
  • Rotatable Bond Count: 4
  • Complexity: 123
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 0
  • Topological Polar Surface Area: 70.3?2

4-(2-methoxyethoxy)pyrimidin-2-amine Pricemore >>

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M139390-10mg
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$ 50.00 2022-06-02
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Additional information on 4-(2-methoxyethoxy)pyrimidin-2-amine

Latest Research Insights on 4-(2-methoxyethoxy)pyrimidin-2-amine (CAS: 852921-87-0) in Chemical Biology and Pharmaceutical Applications

The compound 4-(2-methoxyethoxy)pyrimidin-2-amine (CAS: 852921-87-0) has recently garnered significant attention in the field of chemical biology and pharmaceutical research due to its versatile applications in drug discovery and development. This pyrimidine derivative has been identified as a key intermediate in the synthesis of novel kinase inhibitors, particularly those targeting oncogenic signaling pathways. Recent studies have highlighted its role in the design of selective and potent small-molecule therapeutics, with a focus on cancer and inflammatory diseases.

In a 2023 study published in the Journal of Medicinal Chemistry, researchers demonstrated the efficacy of 4-(2-methoxyethoxy)pyrimidin-2-amine as a building block for the development of next-generation EGFR (Epidermal Growth Factor Receptor) inhibitors. The study revealed that modifications at the 4-position of the pyrimidine ring, including the introduction of the 2-methoxyethoxy moiety, significantly enhanced the compound's binding affinity and selectivity for mutant EGFR isoforms. This finding is particularly relevant for the treatment of non-small cell lung cancer (NSCLC), where EGFR mutations are prevalent.

Another recent investigation, published in Bioorganic & Medicinal Chemistry Letters, explored the compound's potential in modulating immune responses. The researchers synthesized a series of derivatives based on 4-(2-methoxyethoxy)pyrimidin-2-amine and evaluated their effects on T-cell activation. The results indicated that certain derivatives could selectively inhibit JAK3 (Janus Kinase 3), a critical mediator of cytokine signaling, suggesting potential applications in autoimmune disorders such as rheumatoid arthritis and psoriasis.

From a synthetic chemistry perspective, advances in the scalable production of 4-(2-methoxyethoxy)pyrimidin-2-amine have been reported in Organic Process Research & Development. The study described an optimized, cost-effective route for its synthesis, emphasizing green chemistry principles such as reduced solvent usage and improved atom economy. This development is expected to facilitate broader access to the compound for both academic and industrial research.

Ongoing preclinical studies are further investigating the pharmacokinetic and toxicological profiles of 4-(2-methoxyethoxy)pyrimidin-2-amine derivatives. Preliminary data suggest favorable oral bioavailability and manageable toxicity, positioning these compounds as promising candidates for clinical translation. Future research directions may include combination therapies with existing anticancer agents and exploration of their utility in other therapeutic areas, such as neurodegenerative diseases.

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