Cas no 1202645-50-8 (9-Methoxymethyl Guanine)

9-Methoxymethyl Guanine is a modified nucleobase derivative with applications in nucleic acid chemistry and pharmaceutical research. Its key advantage lies in the methoxymethyl group at the 9-position, which enhances solubility and stability compared to unmodified guanine. This modification allows for improved handling in synthetic processes, particularly in oligonucleotide synthesis and prodrug development. The compound serves as a versatile intermediate for designing nucleoside analogs with potential therapeutic activity. Its structural features enable selective functionalization, making it valuable for studying DNA interactions or developing antiviral and anticancer agents. The methoxymethyl group also offers steric and electronic effects that can influence base-pairing properties, useful for probing nucleic acid structure-function relationships.
9-Methoxymethyl Guanine structure
9-Methoxymethyl Guanine structure
Product Name:9-Methoxymethyl Guanine
CAS No:1202645-50-8
MF:C7H9N5O2
MW:195.178660154343
CID:1060454
PubChem ID:136034597
Update Time:2025-11-02

9-Methoxymethyl Guanine Chemical and Physical Properties

Names and Identifiers

    • 2-amino-1,9-dihydro-9-(methoxymethyl)-6H-Purin-6-one
    • 9-Methoxymethyl Guanine
    • 9-Methoxymethyl Guan
    • 1202645-50-8
    • NL3PY28VAD
    • 2-Amino-9-(methoxymethyl)-6,9-dihydro-1H-purin-6-one
    • 2-Amino-1,9-dihydro-9-(methoxymethyl)-6H-purin-6-one; 9-Methoxymethylguanine; Valganciclovir Hydrochloride Imp. C (EP)
    • Valganciclovir Impurity C
    • 2-Amino-9-(methoxymethyl)-9H-purin-6-ol
    • 6H-Purin-6-one, 2-amino-1,9-dihydro-9-(methoxymethyl)-
    • METHOXYMETHYLGUANINE
    • SCHEMBL2343359
    • 2-amino-9-(methoxymethyl)-1H-purin-6-one
    • CS-0165176
    • 2-amino-9-(methoxymethyl)-1H-purin-6(9H)-one? (Ganciclovir Impurity pound(c)
    • 9-Methoxymethylguanine
    • DB-229746
    • METHOXYMETHYLGUANINE [USP-RS]
    • Inchi: 1S/C7H9N5O2/c1-14-3-12-2-9-4-5(12)10-7(8)11-6(4)13/h2H,3H2,1H3,(H3,8,10,11,13)
    • InChI Key: WVWIFQBDNZCHIY-UHFFFAOYSA-N
    • SMILES: O(C)CN1C=NC2C(NC(N)=NC1=2)=O

Computed Properties

  • Exact Mass: 195.076
  • Monoisotopic Mass: 195.076
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 14
  • Rotatable Bond Count: 2
  • Complexity: 279
  • 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: _0.9
  • Topological Polar Surface Area: 94.5A^2

Experimental Properties

  • Color/Form: No data available
  • Density: 1.7±0.1 g/cm3
  • Melting Point: No data available
  • Boiling Point: No data available
  • Flash Point: No data available
  • Vapor Pressure: No data available

9-Methoxymethyl Guanine Security Information

9-Methoxymethyl Guanine Pricemore >>

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Additional information on 9-Methoxymethyl Guanine

9-Methoxymethyl Guanine (CAS No. 1202645-50-8): A Comprehensive Overview of Its Properties and Applications

9-Methoxymethyl Guanine (CAS No. 1202645-50-8) is a modified nucleobase derivative that has garnered significant attention in the fields of medicinal chemistry, biochemistry, and pharmaceutical research. This compound, a guanine analog, is characterized by the presence of a methoxymethyl group at the 9-position, which imparts unique chemical and biological properties. Researchers are increasingly interested in 9-Methoxymethyl Guanine derivatives due to their potential applications in drug development, nucleic acid research, and diagnostic tools.

The molecular structure of 9-Methoxymethyl Guanine features a guanine core with a methoxymethyl substituent, making it a valuable building block for synthetic nucleic acids. This modification enhances the compound's stability and solubility, which are critical factors in its utility across various scientific applications. The CAS 1202645-50-8 compound is particularly notable for its role in studying DNA repair mechanisms and epigenetic modifications, areas that are currently at the forefront of biomedical research.

In recent years, the demand for 9-Methoxymethyl Guanine analogs has surged, driven by advancements in personalized medicine and targeted therapies. The compound's ability to mimic natural nucleobases while offering improved pharmacokinetic properties makes it a promising candidate for the development of novel therapeutics. For instance, researchers are exploring its use in the design of antiviral and anticancer agents, where precise molecular targeting is essential.

From a synthetic perspective, 9-Methoxymethyl Guanine is often utilized in oligonucleotide synthesis to introduce specific modifications that enhance binding affinity or resistance to enzymatic degradation. This has significant implications for the development of antisense oligonucleotides and siRNA-based therapies, which are revolutionizing the treatment of genetic disorders and viral infections. The 1202645-50-8 chemical is also employed in the study of nucleic acid-protein interactions, providing insights into fundamental biological processes.

The pharmaceutical industry has shown growing interest in 9-Methoxymethyl Guanine-based compounds due to their potential to improve drug delivery systems. Its modified structure allows for better bioavailability and reduced toxicity, addressing some of the key challenges in drug formulation. Additionally, the compound's compatibility with various analytical techniques, such as HPLC and mass spectrometry, facilitates its characterization and quality control in research and production settings.

Beyond its therapeutic applications, 9-Methoxymethyl Guanine (CAS No. 1202645-50-8) is also valuable in diagnostic assays and biomarker research. Its unique chemical properties enable the development of sensitive and specific detection methods for nucleic acid sequences, which are crucial for early disease diagnosis and monitoring. The compound's versatility extends to materials science, where it is used to engineer functional nanomaterials with applications in biosensing and nanotechnology.

In conclusion, 9-Methoxymethyl Guanine represents a versatile and highly functionalized nucleobase derivative with wide-ranging applications in science and medicine. Its distinct structural features and biological relevance make it a subject of ongoing research and innovation. As the scientific community continues to explore its potential, the CAS 1202645-50-8 compound is poised to play a pivotal role in advancing our understanding of nucleic acid chemistry and its therapeutic applications.

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