Cas no 761339-87-1 (N1-(4-Methylpyrimidin-2-yl)ethane-1,2-diamine)

N1-(4-Methylpyrimidin-2-yl)ethane-1,2-diamine is a pyrimidine derivative featuring a primary amine and a secondary amine functional group, making it a versatile intermediate in organic synthesis and pharmaceutical applications. Its structure allows for selective reactivity in nucleophilic substitution and condensation reactions, particularly in the development of heterocyclic compounds. The 4-methyl substituent enhances stability while maintaining reactivity, offering advantages in controlled functionalization. This compound is commonly employed in the synthesis of bioactive molecules, including potential kinase inhibitors and antimicrobial agents. Its well-defined purity and consistent performance make it suitable for research and industrial-scale applications requiring precise molecular modifications.
N1-(4-Methylpyrimidin-2-yl)ethane-1,2-diamine structure
761339-87-1 structure
Product Name:N1-(4-Methylpyrimidin-2-yl)ethane-1,2-diamine
CAS No:761339-87-1
MF:C7H12N4
MW:152.196980476379
MDL:MFCD17258726
CID:550014
PubChem ID:45091774
Update Time:2025-05-20

N1-(4-Methylpyrimidin-2-yl)ethane-1,2-diamine Chemical and Physical Properties

Names and Identifiers

    • 1,2-Ethanediamine,N1-(4-methyl-2-pyrimidinyl)-
    • 1,2-Ethanediamine,N-(4-methyl-2-pyrimidinyl)- (9CI)
    • N1-(4-Methylpyrimidin-2-yl)ethane-1,2-diamine
    • MDL: MFCD17258726
    • Inchi: 1S/C7H12N4/c1-6-2-4-9-7(11-6)10-5-3-8/h2,4H,3,5,8H2,1H3,(H,9,10,11)
    • InChI Key: MHNLIVPBRUYPEX-UHFFFAOYSA-N
    • SMILES: N(C1N=CC=C(C)N=1)CCN

Computed Properties

  • Exact Mass: 152.106
  • Monoisotopic Mass: 152.106
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 11
  • Rotatable Bond Count: 3
  • Complexity: 107
  • 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
  • Topological Polar Surface Area: 63.8

N1-(4-Methylpyrimidin-2-yl)ethane-1,2-diamine Pricemore >>

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N1-(4-Methylpyrimidin-2-yl)ethane-1,2-diamine Related Literature

Additional information on N1-(4-Methylpyrimidin-2-yl)ethane-1,2-diamine

Research Brief on N1-(4-Methylpyrimidin-2-yl)ethane-1,2-diamine (CAS: 761339-87-1): Recent Advances and Applications

N1-(4-Methylpyrimidin-2-yl)ethane-1,2-diamine (CAS: 761339-87-1) is a structurally unique compound that has garnered significant attention in the field of chemical biology and medicinal chemistry. Recent studies have explored its potential as a key intermediate in the synthesis of novel therapeutic agents, particularly in the development of kinase inhibitors and antimicrobial compounds. This research brief aims to summarize the latest findings related to this compound, highlighting its synthetic pathways, biological activities, and potential applications in drug discovery.

One of the most notable advancements in the study of N1-(4-Methylpyrimidin-2-yl)ethane-1,2-diamine is its role in the synthesis of pyrimidine-based kinase inhibitors. A 2023 study published in the Journal of Medicinal Chemistry demonstrated that derivatives of this compound exhibit potent inhibitory activity against cyclin-dependent kinases (CDKs), which are critical targets in cancer therapy. The researchers utilized a structure-activity relationship (SAR) approach to optimize the compound's binding affinity, resulting in derivatives with nanomolar potency against CDK2 and CDK4.

In addition to its applications in oncology, N1-(4-Methylpyrimidin-2-yl)ethane-1,2-diamine has shown promise in antimicrobial research. A recent preprint on BioRxiv reported that this compound serves as a scaffold for the development of novel antibiotics targeting multidrug-resistant Gram-negative bacteria. The study highlighted its ability to disrupt bacterial cell wall synthesis by inhibiting key enzymes involved in peptidoglycan biosynthesis. These findings underscore the compound's versatility and potential to address pressing global health challenges.

The synthetic accessibility of N1-(4-Methylpyrimidin-2-yl)ethane-1,2-diamine has also been a focal point of recent research. A 2022 paper in Organic Letters detailed an efficient, one-pot synthesis method that significantly improves yield and reduces production costs. This methodological advancement is expected to facilitate broader adoption of the compound in both academic and industrial settings, enabling more extensive exploration of its pharmacological properties.

Despite these promising developments, challenges remain in the clinical translation of N1-(4-Methylpyrimidin-2-yl)ethane-1,2-diamine-based therapeutics. Pharmacokinetic studies indicate that further optimization is needed to enhance bioavailability and reduce off-target effects. Ongoing research is investigating prodrug strategies and formulation technologies to overcome these limitations, with preliminary results showing improved plasma stability in animal models.

In conclusion, N1-(4-Methylpyrimidin-2-yl)ethane-1,2-diamine (CAS: 761339-87-1) represents a valuable chemical entity with diverse applications in drug discovery. Its role in kinase inhibition and antimicrobial activity, coupled with recent synthetic advancements, positions it as a compound of significant interest for future therapeutic development. Continued research efforts will be crucial to fully realize its potential in addressing unmet medical needs.

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