Cas no 697762-17-7 (Zinc, chloro[(2,3-dichlorophenyl)methyl]-)

Zinc, chloro[(2,3-dichlorophenyl)methyl]-, is an organozinc compound characterized by its unique structural and reactive properties. This chemical features a zinc center coordinated to a chloro ligand and a (2,3-dichlorophenyl)methyl group, making it a versatile intermediate in organic synthesis. Its stability and reactivity under controlled conditions enable its use in cross-coupling reactions, such as Negishi coupling, where it facilitates the formation of carbon-carbon bonds. The presence of dichlorophenyl substituents enhances its selectivity in transformations involving aromatic systems. This compound is particularly valued for its efficiency in constructing complex molecular frameworks, making it a useful tool in pharmaceutical and fine chemical research. Proper handling under inert conditions is recommended due to its sensitivity to air and moisture.
Zinc, chloro[(2,3-dichlorophenyl)methyl]- structure
697762-17-7 structure
Product Name:Zinc, chloro[(2,3-dichlorophenyl)methyl]-
CAS No:697762-17-7
MF:C7H5Cl3Zn
MW:260.882595777512
MDL:MFCD22684859
CID:4150742
PubChem ID:58801797
Update Time:2025-06-12

Zinc, chloro[(2,3-dichlorophenyl)methyl]- Chemical and Physical Properties

Names and Identifiers

    • Zinc, chloro[(2,3-dichlorophenyl)methyl]-
    • 2,3-Dichlorobenzylzinc chloride
    • chlorozinc(1+);1,2-dichloro-3-methanidylbenzene
    • 2,3-Dichlorobenzylzinc chloride, 0.50 M in THF
    • MFCD22684859
    • 697762-17-7
    • MDL: MFCD22684859
    • Inchi: 1S/C7H5Cl2.ClH.Zn/c1-5-3-2-4-6(8)7(5)9;;/h2-4H,1H2;1H;/q;;+1/p-1
    • InChI Key: IGDWQMQFZANWFT-UHFFFAOYSA-M
    • SMILES: C(C1C=CC=C(Cl)C=1Cl)[Zn]Cl

Computed Properties

  • Exact Mass: 257.874825Da
  • Monoisotopic Mass: 257.874825Da
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 1
  • Heavy Atom Count: 11
  • Rotatable Bond Count: 0
  • Complexity: 99.7
  • 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
  • Topological Polar Surface Area: 0?2

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Zinc, chloro[(2,3-dichlorophenyl)methyl]- Suppliers

Amadis Chemical Company Limited
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(CAS:697762-17-7)Zinc, chloro[(2,3-dichlorophenyl)methyl]-
Order Number:A1172720
Stock Status:in Stock
Quantity:50ml/100ml
Purity:99%
Pricing Information Last Updated:Friday, 30 August 2024 01:23
Price ($):684.0/1072.0

Additional information on Zinc, chloro[(2,3-dichlorophenyl)methyl]-

Professional Introduction to Zinc, chloro[(2,3-dichlorophenyl)methyl]- (CAS No. 697762-17-7)

Zinc, chloro[(2,3-dichlorophenyl)methyl]-, a compound with the CAS number 697762-17-7, represents a significant advancement in the field of organometallic chemistry and its applications in pharmaceutical research. This organozinc reagent is characterized by its unique structural properties, which make it a valuable tool in synthetic chemistry. The presence of a chloro substituent and a (2,3-dichlorophenyl)methyl group imparts specific reactivity that is highly beneficial in the synthesis of complex molecules.

The compound's molecular structure is pivotal in understanding its utility. The zinc center, coordinated to a chloro group and a phenyl ring substituted with two chlorine atoms at the 2 and 3 positions, creates a highly reactive species. This reactivity is exploited in various synthetic pathways, particularly in cross-coupling reactions such as the Suzuki-Miyaura and Heck reactions. These reactions are fundamental in constructing carbon-carbon bonds, which are essential in the development of novel pharmaceuticals.

In recent years, there has been a surge in research focused on developing efficient and sustainable methods for drug synthesis. Zinc-based reagents have emerged as promising candidates due to their relatively low toxicity and high efficiency. Zinc, chloro[(2,3-dichlorophenyl)methyl]- has been extensively studied for its role in facilitating these reactions under mild conditions. This characteristic is particularly advantageous in pharmaceutical applications where harsh reaction conditions can lead to the formation of unwanted byproducts.

The use of this compound has been highlighted in several cutting-edge studies. For instance, researchers have utilized Zinc, chloro[(2,3-dichlorophenyl)methyl]- to synthesize novel heterocyclic compounds that exhibit significant biological activity. These studies have demonstrated the compound's ability to act as a bridge between different molecular fragments, enabling the construction of complex structures with high precision. Such advancements are crucial for the development of next-generation therapeutics that target various diseases more effectively.

The compound's versatility extends beyond its role as a synthetic intermediate. It has also been explored for its potential in catalytic systems where it can enhance reaction rates without being consumed in the process. This property makes it an attractive option for industrial-scale applications where efficiency and cost-effectiveness are paramount. Moreover, its stability under various reaction conditions further adds to its appeal as a reliable reagent.

Recent innovations in chemical biology have also leveraged Zinc, chloro[(2,3-dichlorophenyl)methyl]- to develop novel probes for studying biological pathways. By incorporating this compound into bioactive molecules, researchers can gain insights into the mechanisms of various cellular processes. This approach has opened up new avenues for drug discovery by allowing scientists to design molecules that interact specifically with target proteins or enzymes.

The environmental impact of using Zinc-based reagents has also been a point of interest. Unlike some traditional metal catalysts that require harsh conditions or generate hazardous waste, Zinc, chloro[(2,3-dichlorophenyl)methyl]- offers a more sustainable alternative. Its ability to participate in reactions under ambient conditions reduces the need for energy-intensive processes and minimizes waste generation. This aligns with global efforts to promote green chemistry and sustainable practices in the pharmaceutical industry.

In conclusion, Zinc, chloro[(2,3-dichlorophenyl)methyl]- (CAS No. 697762-17-7) is a multifaceted compound with significant implications for both academic research and industrial applications. Its unique structural features and reactivity make it an invaluable tool in synthetic chemistry, particularly in the development of novel pharmaceuticals. As research continues to evolve, this compound is expected to play an even greater role in advancing chemical biology and drug discovery efforts worldwide.

Recommended suppliers
Amadis Chemical Company Limited
(CAS:697762-17-7)Zinc, chloro[(2,3-dichlorophenyl)methyl]-
A1172720
Purity:99%/99%
Quantity:50ml/100ml
Price ($):684.0/1072.0
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