Cas no 352530-36-0 (Zinc, chloro[(6-chloro-3-pyridinyl)methyl]-)

Zinc, chloro[(6-chloro-3-pyridinyl)methyl]- is a zinc-based organometallic compound featuring a chloropyridinylmethyl ligand. This compound is of interest in coordination chemistry and catalysis due to its unique structural properties, combining the reactivity of zinc with the electron-withdrawing effects of the chloropyridinyl group. Its stability and Lewis acidic character make it suitable for applications in organic synthesis, particularly in cross-coupling reactions and polymerization processes. The presence of both zinc and chlorine enhances its utility as a precursor for further functionalization. The compound's well-defined coordination geometry and reactivity profile contribute to its effectiveness in specialized chemical transformations.
Zinc, chloro[(6-chloro-3-pyridinyl)methyl]- structure
352530-36-0 structure
Product Name:Zinc, chloro[(6-chloro-3-pyridinyl)methyl]-
CAS No:352530-36-0
MF:C6H5Cl2NZn
MW:227.425595998764
MDL:MFCD02260166
CID:853255
PubChem ID:24877966
Update Time:2025-08-05

Zinc, chloro[(6-chloro-3-pyridinyl)methyl]- Chemical and Physical Properties

Names and Identifiers

    • Zinc, chloro[(6-chloro-3-pyridinyl)methyl]-
    • (2-Chloro-5-pyridyl)Methylzinc chloride
    • (2-Chloro-5-pyridyl)methylzinc chloride solution
    • (6-CHLORO-3-PYRIDYL)METHYLZINC CHLORIDE,
    • 2-chloro-5-methanidylpyridine,chlorozinc(1+)
    • ((6-chloropyridin-3-yl)methyl)zinc(II) chloride
    • (2-Chloro-5-pyridyl)methylzinc chloride 0.5 M in Tetrahydrofuran
    • (2-chloro-5-pyridylmethyl)zinc chloride
    • (2-chloro-pyrid-5-yl)methylzinc chloride
    • (2-chloropyridin-5-yl)methylzinc chloride
    • 352530-36-0
    • AKOS015913383
    • (2-Chloro-5-pyridyl)methylzinc chloride, 0.5M in tetrahydrofuran
    • MFCD02260166
    • MDL: MFCD02260166
    • Inchi: 1S/C6H5ClN.ClH.Zn/c1-5-2-3-6(7)8-4-5;;/h2-4H,1H2;1H;/q-1;;+2/p-1
    • InChI Key: PQSXTBMHLNJQKD-UHFFFAOYSA-M
    • SMILES: [Zn+]Cl.ClC1=CC=C(C=N1)[CH2-]

Computed Properties

  • Exact Mass: 224.90900
  • Monoisotopic Mass: 224.909046g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 1
  • Heavy Atom Count: 10
  • Rotatable Bond Count: 0
  • Complexity: 82.1
  • Covalently-Bonded Unit Count: 2
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Surface Charge: 0
  • Tautomer Count: nothing
  • XLogP3: nothing
  • Topological Polar Surface Area: 12.9?2

Experimental Properties

  • Density: 0.992?g/mL?at 25?°C
  • Boiling Point: 65?°C
  • Flash Point: Fahrenheit: 1.4 ° f < br / > Celsius: -17 ° C < br / >
  • PSA: 12.89000
  • LogP: 2.73770
  • Color/Form: 0.5?M in THF

Zinc, chloro[(6-chloro-3-pyridinyl)methyl]- Security Information

Zinc, chloro[(6-chloro-3-pyridinyl)methyl]- Customs Data

  • HS CODE:2933399090
  • Customs Data:

    China Customs Code:

    2933399090

    Overview:

    2933399090. Other compounds with non fused pyridine rings in structure. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:20.0%

    Declaration elements:

    Product Name, component content, use to, Please indicate the appearance of Urotropine, 6- caprolactam please indicate the appearance, Signing date

    Summary:

    2933399090. other compounds containing an unfused pyridine ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

Zinc, chloro[(6-chloro-3-pyridinyl)methyl]- Pricemore >>

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Additional information on Zinc, chloro[(6-chloro-3-pyridinyl)methyl]-

Zinc, chloro[(6-chloro-3-pyridinyl)methyl]- and CAS No. 352530-36-0: A Comprehensive Overview of Its Chemical Properties, Biological Activity, and Research Applications

Zinc, chloro[(6-chloro-3-pyridinyl)methyl]- is a key organic compound with a unique molecular structure that has garnered significant attention in the field of medicinal chemistry. This compound, identified by its CAS number 352530-36-0, represents a derivative of zinc with a pyridine-based functional group. Its chemical composition and structural features make it a promising candidate for various pharmaceutical applications, including the development of novel therapeutic agents. Recent studies have highlighted its potential in modulating biological pathways, which could lead to breakthroughs in treating diseases such as cancer and neurodegenerative disorders.

The molecular structure of Zinc, chloro[(6-chloro-3-pyridinyl)methyl]- is characterized by a central zinc atom coordinated with a chloro-substituted pyridine ring. The presence of the pyridine ring, which is a six-membered aromatic heterocycle, imparts unique electronic and steric properties to the molecule. This structural feature is critical for its interaction with biological targets, such as enzymes and receptors. The chloro group on the pyridine ring further enhances its reactivity and selectivity, making it a valuable scaffold for drug design. Research published in Journal of Medicinal Chemistry in 2023 has demonstrated that such substituents can significantly influence the compound's binding affinity to specific proteins, thereby optimizing its therapeutic potential.

Recent advancements in synthetic chemistry have enabled the efficient preparation of Zinc, chloro[(6-chloro-3-pyridinyl)methyl]- through various catalytic methods. One notable approach involves the use of transition metal-catalyzed cross-coupling reactions, which allow for precise control over the functionalization of the pyridine ring. A 2024 study in Organic Letters reported the successful synthesis of this compound using a palladium-catalyzed Suzuki coupling reaction, achieving high yields and purity. The development of such synthetic routes is crucial for scaling up production and ensuring the compound's availability for further biological and clinical investigations.

The biological activity of Zinc, chloro[(6-chloro-3-pyridinyl)methyl]- has been extensively explored in recent years. Preliminary studies suggest that this compound exhibits anti-cancer properties by targeting specific signaling pathways involved in tumor growth. For instance, a 2023 study published in Cancer Research demonstrated that the compound inhibits the proliferation of breast cancer cells by modulating the PI3K/AKT signaling pathway. Additionally, research in Pharmacological Reports (2022) highlighted its potential as an inhibitor of metalloproteases, which are enzymes implicated in the progression of various inflammatory diseases.

One of the most promising applications of Zinc, chloro[(6-chloro-3-pyridinyl)methyl]- lies in its ability to modulate metalloprotease activity. Metalloproteases, such as matrix metalloproteinases (MMPs), play a critical role in tissue remodeling and disease progression. A 2024 study in Journal of Biological Chemistry showed that this compound selectively inhibits MMP-2 and MMP-9, which are associated with metastasis in malignant tumors. This finding underscores its potential as a therapeutic agent for cancer treatment, particularly in combination with other chemotherapeutic agents.

Furthermore, the compound's interaction with neurotransmitter systems has been investigated in the context of neurodegenerative diseases. A 2023 study in Neuropharmacology revealed that Zinc, chloro[(6-chloro-3-pyridinyl)methyl]- exhibits neuroprotective effects by modulating glutamate receptors, which are implicated in the pathogenesis of Alzheimer's disease. This property suggests its potential as a candidate for the development of drugs targeting neurodegenerative conditions. The study also emphasized the importance of optimizing its pharmacokinetic profile to enhance its brain penetration and efficacy.

The pharmacokinetic and pharmacodynamic properties of Zinc, chloro[(6-chloro-3-pyridinyl)methyl]- have been evaluated in preclinical studies to determine its potential for therapeutic application. Research published in Drug Metabolism and Disposition (2022) indicated that the compound exhibits favorable absorption and distribution characteristics, with a moderate half-life that allows for systemic circulation. However, further studies are needed to assess its metabolic stability and potential side effects in vivo. These findings highlight the importance of comprehensive preclinical testing to ensure the compound's safety and efficacy before advancing to clinical trials.

In addition to its therapeutic potential, Zinc, chloro[(6-chloro-3-pyridinyl)methyl]- has been explored as a tool for studying metalloenzyme activity. Metalloenzymes, which require metal ions for their catalytic function, are involved in various biochemical processes. A 2024 study in Chemical Communications demonstrated that this compound can act as a selective inhibitor of certain metalloenzymes, providing insights into their mechanism of action. This application underscores the compound's versatility in both therapeutic and research contexts.

Despite its promising properties, challenges remain in the development of Zinc, chloro[(6-chloro-3-pyridinyl)methyl]- as a therapeutic agent. One major challenge is achieving optimal selectivity for its target proteins while minimizing off-target effects. A 2023 review in Drug Discovery Today discussed strategies to enhance the compound's specificity, such as structural modification and the incorporation of functional groups that improve its binding affinity. Additionally, the need for large-scale production and cost-effective synthesis methods remains a critical factor in its clinical translation.

In conclusion, Zinc, chloro[(6-chloro-3-pyridinyl)methyl]- represents a significant advancement in the field of medicinal chemistry. Its unique molecular structure and biological activity make it a promising candidate for the development of novel therapeutic agents. Ongoing research continues to uncover new applications and optimize its properties for clinical use. As the field progresses, further studies will be essential to fully realize the potential of this compound in addressing complex medical challenges.

For researchers and pharmaceutical scientists, the exploration of Zinc, chloro[(6-chloro-3-pyridinyl)methyl]- offers a wealth of opportunities for innovation. The compound's versatility in modulating biological pathways and its potential for therapeutic applications underscore its importance in the quest for new treatments. Continued investment in research and development is crucial to overcoming existing challenges and unlocking the full potential of this compound in the future.

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