Cas no 142228-52-2 (Methyl(4,6-dichloro-2-methylpyrimidin-5-yl)acetate)

Methyl(4,6-dichloro-2-methylpyrimidin-5-yl)acetate is a versatile pyrimidine derivative widely used as a key intermediate in organic synthesis and pharmaceutical applications. Its structure features reactive chloro and ester functional groups, enabling further modifications such as nucleophilic substitutions or condensations. The compound exhibits high purity and stability, making it suitable for precise synthetic routes in agrochemical and medicinal chemistry. Its methylpyrimidine core is particularly valuable for constructing heterocyclic frameworks. The dichloro substitution pattern enhances reactivity, facilitating selective transformations. This ester derivative is favored for its compatibility with a range of reaction conditions, offering synthetic flexibility in the development of advanced chemical entities.
Methyl(4,6-dichloro-2-methylpyrimidin-5-yl)acetate structure
142228-52-2 structure
Product Name:Methyl(4,6-dichloro-2-methylpyrimidin-5-yl)acetate
CAS No:142228-52-2
MF:C8H8Cl2N2O2
MW:235.067319869995
MDL:MFCD11870529
CID:2126457
Update Time:2025-10-29

Methyl(4,6-dichloro-2-methylpyrimidin-5-yl)acetate Chemical and Physical Properties

Names and Identifiers

    • methyl 2-(4,6-dichloro-2-methyl-pyrimidin-5-yl)-acetate
    • Methyl 2-(4,6-dichloro-2-methylpyrimidin-5-yl)acetate
    • SYVXDRVDBGASGV-UHFFFAOYSA-N
    • methyl(4,6-dichloro-2-methylpyrimidin-5-yl)acetate
    • Methyl 4,6-dichloro-2-methyl-pyrimidin-5-yl-acetate
    • methyl (4,6-dichloro-2-methylpyrimidin-5-yl)acetate
    • methyl (4,6-dichloro-2-methyl-pyrimidin-5-yl )-acetate
    • 4,6-dichloro-2-methylpyrimidine-5-acetic acid, methyl ester
    • Methyl(4,6-dichloro-2-methylpyrimidin-5-yl)acetate
    • MDL: MFCD11870529
    • Inchi: 1S/C8H8Cl2N2O2/c1-4-11-7(9)5(8(10)12-4)3-6(13)14-2/h3H2,1-2H3
    • InChI Key: SYVXDRVDBGASGV-UHFFFAOYSA-N
    • SMILES: ClC1C(=C(N=C(C)N=1)Cl)CC(=O)OC

Computed Properties

  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 14
  • Rotatable Bond Count: 3
  • Complexity: 204
  • Topological Polar Surface Area: 52.1

Methyl(4,6-dichloro-2-methylpyrimidin-5-yl)acetate Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
Matrix Scientific
208537-1g
Methyl 2-(4,6-dichloro-2-methyl-pyrimidin-5-yl)acetate
142228-52-2
1g
$794.00 2023-09-06

Methyl(4,6-dichloro-2-methylpyrimidin-5-yl)acetate Related Literature

Additional information on Methyl(4,6-dichloro-2-methylpyrimidin-5-yl)acetate

Recent Advances in the Study of Methyl(4,6-dichloro-2-methylpyrimidin-5-yl)acetate (CAS: 142228-52-2)

Methyl(4,6-dichloro-2-methylpyrimidin-5-yl)acetate (CAS: 142228-52-2) 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 synthesis. This research brief aims to provide an overview of the latest findings related to this compound, focusing on its applications, synthesis methods, and biological activities.

One of the most notable advancements in the study of Methyl(4,6-dichloro-2-methylpyrimidin-5-yl)acetate is its application in the synthesis of pyrimidine-based drugs. Pyrimidine derivatives are known for their diverse pharmacological properties, including antiviral, anticancer, and anti-inflammatory activities. Recent research has demonstrated that this compound serves as a versatile building block for the development of such derivatives, enabling the creation of more potent and selective therapeutic agents.

In terms of synthesis, recent studies have explored more efficient and environmentally friendly methods for producing Methyl(4,6-dichloro-2-methylpyrimidin-5-yl)acetate. Traditional synthetic routes often involve harsh conditions and generate significant waste. However, newer approaches, such as catalytic methods and green chemistry techniques, have shown promise in improving yield and reducing environmental impact. These advancements are particularly relevant given the increasing emphasis on sustainable practices in chemical manufacturing.

Biological studies have also shed light on the potential mechanisms of action of compounds derived from Methyl(4,6-dichloro-2-methylpyrimidin-5-yl)acetate. For instance, some derivatives have been found to inhibit specific enzymes involved in disease pathways, offering new targets for drug development. Additionally, structure-activity relationship (SAR) studies have provided valuable insights into how modifications to the pyrimidine core can enhance biological activity and reduce toxicity.

Despite these promising developments, challenges remain in the widespread application of Methyl(4,6-dichloro-2-methylpyrimidin-5-yl)acetate. Issues such as scalability, cost-effectiveness, and regulatory approval need to be addressed to fully realize its potential. Future research directions may include further optimization of synthetic routes, expanded biological testing, and exploration of new applications in drug discovery and beyond.

In conclusion, Methyl(4,6-dichloro-2-methylpyrimidin-5-yl)acetate continues to be a compound of significant interest in the field of chemical biology and medicinal chemistry. Its versatility as a synthetic intermediate and its potential in drug development make it a valuable focus for ongoing research. By addressing current challenges and leveraging recent advancements, researchers can unlock new opportunities for innovation in this area.

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