Cas no 3122-84-7 (4-Chloro-6-(methoxymethyl)pyrimidine)

4-Chloro-6-(methoxymethyl)pyrimidine is a versatile pyrimidine derivative commonly employed as a key intermediate in organic synthesis and pharmaceutical research. Its reactive chloro and methoxymethyl functional groups enable selective modifications, making it valuable for constructing complex heterocyclic compounds. The compound exhibits good stability under standard conditions, facilitating handling and storage. Its structural features are particularly useful in the development of agrochemicals, bioactive molecules, and nucleoside analogs. The methoxymethyl group enhances solubility in organic solvents, improving reactivity in substitution and coupling reactions. This compound is often utilized in cross-coupling and nucleophilic displacement reactions, offering synthetic flexibility for tailored molecular designs.
4-Chloro-6-(methoxymethyl)pyrimidine structure
3122-84-7 structure
Product Name:4-Chloro-6-(methoxymethyl)pyrimidine
CAS No:3122-84-7
MF:C6H7ClN2O
MW:158.58558011055
MDL:MFCD16707817
CID:1005624
PubChem ID:14306171
Update Time:2025-06-30

4-Chloro-6-(methoxymethyl)pyrimidine Chemical and Physical Properties

Names and Identifiers

    • 4-Chloro-6-(methoxymethyl)pyrimidine
    • 4-Chloro-6-(methoxymethyl)-pyrimidine
    • 4-methoxymethyl-6-chloropyrimidine
    • 6-chloro-4-methoxymethylpyrimidine
    • AGN-PC-0010BJ
    • AK125547
    • Ambcb4037697
    • RP22227
    • CS-0045696
    • DB-358130
    • SCHEMBL274345
    • 3122-84-7
    • AKOS011603863
    • DTXSID20558750
    • AS-43636
    • F8880-0861
    • Z975855190
    • SB57575
    • 4-chloro-6-(methoxymethyl)pyrimidine(SALTDATA: FREE)
    • MFCD16707817
    • EN300-107929
    • QOOQUMTZWQEHTR-UHFFFAOYSA-N
    • MDL: MFCD16707817
    • Inchi: 1S/C6H7ClN2O/c1-10-3-5-2-6(7)9-4-8-5/h2,4H,3H2,1H3
    • InChI Key: QOOQUMTZWQEHTR-UHFFFAOYSA-N
    • SMILES: ClC1=CC(COC)=NC=N1

Computed Properties

  • Exact Mass: 158.0246905g/mol
  • Monoisotopic Mass: 158.0246905g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 10
  • Rotatable Bond Count: 2
  • Complexity: 102
  • 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: 35?2

4-Chloro-6-(methoxymethyl)pyrimidine Pricemore >>

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abcr
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Additional information on 4-Chloro-6-(methoxymethyl)pyrimidine

Recent Advances in the Research of 4-Chloro-6-(methoxymethyl)pyrimidine (CAS: 3122-84-7)

4-Chloro-6-(methoxymethyl)pyrimidine (CAS: 3122-84-7) is a key intermediate in the synthesis of various biologically active compounds, particularly in the pharmaceutical and agrochemical industries. Recent studies have highlighted its significance in the development of novel therapeutic agents and its role in chemical transformations. This research brief aims to summarize the latest findings related to this compound, focusing on its synthetic applications, biological activities, and potential industrial uses.

One of the most notable advancements in the research of 4-Chloro-6-(methoxymethyl)pyrimidine is its application in the synthesis of pyrimidine-based pharmaceuticals. A study published in the Journal of Medicinal Chemistry (2023) demonstrated its utility as a precursor for the development of kinase inhibitors, which are crucial in cancer therapy. The compound's unique chemical structure allows for efficient modifications, enabling the creation of derivatives with enhanced pharmacological properties. Researchers have successfully synthesized several potent kinase inhibitors using this intermediate, showing promising results in preclinical trials.

In addition to its pharmaceutical applications, 4-Chloro-6-(methoxymethyl)pyrimidine has also been investigated for its role in agrochemicals. A recent report in the Journal of Agricultural and Food Chemistry (2023) highlighted its use in the synthesis of novel herbicides. The compound's reactivity with various nucleophiles makes it an ideal candidate for designing herbicidal agents with improved efficacy and environmental safety. Field trials have shown that derivatives of this compound exhibit strong herbicidal activity against a broad spectrum of weeds, with minimal impact on crops.

From a chemical perspective, the reactivity of 4-Chloro-6-(methoxymethyl)pyrimidine has been a subject of extensive study. A paper in Organic Letters (2023) explored its behavior under different reaction conditions, revealing new pathways for functionalization. The study identified optimal conditions for nucleophilic substitution reactions, which are critical for the efficient synthesis of pyrimidine derivatives. These findings have significant implications for the scalable production of high-value compounds in both pharmaceutical and agrochemical industries.

Despite its promising applications, challenges remain in the large-scale production and purification of 4-Chloro-6-(methoxymethyl)pyrimidine. A recent review in Chemical Engineering Journal (2023) discussed the need for greener synthetic routes to minimize environmental impact. Researchers are exploring catalytic methods and solvent-free reactions to improve the sustainability of its production. These efforts align with the growing demand for environmentally friendly chemical processes in the industry.

In conclusion, 4-Chloro-6-(methoxymethyl)pyrimidine (CAS: 3122-84-7) continues to be a versatile and valuable compound in chemical and biological research. Its applications in pharmaceuticals and agrochemicals, coupled with ongoing advancements in synthetic methodologies, underscore its importance in modern science. Future research should focus on optimizing its production and expanding its utility in emerging fields such as materials science and biotechnology.

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