Cas no 874-72-6 (Magnesium, chloro[(4-chlorophenyl)methyl]-)

Magnesium, chloro[(4-chlorophenyl)methyl]-, is an organomagnesium compound commonly utilized in Grignard reactions and other synthetic organic chemistry applications. Its key advantages include high reactivity as a nucleophile, enabling the formation of carbon-carbon bonds with electrophiles such as carbonyl compounds. The presence of the 4-chlorophenyl group enhances its stability and selectivity in certain transformations. This reagent is particularly valuable in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals, where precise functionalization is required. It is typically handled under inert conditions due to its sensitivity to moisture and air. Proper storage and handling ensure consistent performance in demanding synthetic workflows.
Magnesium, chloro[(4-chlorophenyl)methyl]- structure
874-72-6 structure
Product Name:Magnesium, chloro[(4-chlorophenyl)methyl]-
CAS No:874-72-6
MF:C7H6Cl2Mg
MW:185.333540439606
MDL:MFCD01311474
CID:656020
PubChem ID:10867043
Update Time:2025-06-10

Magnesium, chloro[(4-chlorophenyl)methyl]- Chemical and Physical Properties

Names and Identifiers

    • Magnesium, chloro[(4-chlorophenyl)methyl]-
    • 4-Chlorobenzylmagnesium chloride
    • magnesium,1-chloro-4-methanidylbenzene,chloride
    • 4-Chlorobenzylmagnesium chloride 0.25 M in Diethyl Ether
    • 4-ChlorobenzylMagnesiuM chloride, 0.50M in 2-Me-THF
    • p-chlorobenzyl magnesium chloride
    • p-ClC6H4CH2MgCl
    • 4-Chlorobenzylmagnesium chloride, 0.50 M in 2-MeTHF
    • DTXSID40446382
    • p-chlorobenzylmagnesium chloride
    • AKOS016017899
    • 874-72-6
    • MFCD01311474
    • A937232
    • SCHEMBL1141849
    • magnesium;1-chloro-4-methanidylbenzene;chloride
    • Magnesium chloride (4-chlorophenyl)methanide (1/1/1)
    • 4-Chlorobenzylmagnesium chloride, 0.50 M in Ether
    • CCGGTOGOFBBGSC-UHFFFAOYSA-M
    • DB-218866
    • MDL: MFCD01311474
    • Inchi: 1S/C7H6Cl.ClH.Mg/c1-6-2-4-7(8)5-3-6;;/h2-5H,1H2;1H;/q-1;;+2/p-1
    • InChI Key: GVNSCNGKEXNKBU-UHFFFAOYSA-M
    • SMILES: ClC1C=CC(=CC=1)[CH2-].[Cl-].[Mg+2]

Computed Properties

  • Exact Mass: 183.97000
  • Monoisotopic Mass: 183.9696973g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 0
  • Heavy Atom Count: 10
  • Rotatable Bond Count: 0
  • Complexity: 70
  • Covalently-Bonded Unit Count: 3
  • 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

Experimental Properties

  • Melting Point: N/A℃
  • Solubility: Miscible with tetrahydrofuran.
  • PSA: 0.00000
  • LogP: 3.34520
  • Sensitiveness: Air & Moisture Sensitive

Magnesium, chloro[(4-chlorophenyl)methyl]- Security Information

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Additional information on Magnesium, chloro[(4-chlorophenyl)methyl]-

Magnesium, chloro[(4-chlorophenyl)methyl]- (CAS No. 874-72-6): A Comprehensive Overview

Magnesium, chloro[(4-chlorophenyl)methyl]-, identified by its CAS number 874-72-6, is a significant compound in the field of organic chemistry and pharmaceutical research. This organomagnesium reagent, characterized by its unique structural and chemical properties, has garnered considerable attention due to its utility in synthetic chemistry and potential applications in medicinal chemistry. The compound's structure, featuring a magnesium center coordinated with a chloro group and a [(4-chlorophenyl)methyl] group, makes it a versatile intermediate in the synthesis of more complex molecules.

The synthesis and handling of Magnesium, chloro[(4-chlorophenyl)methyl]- require meticulous attention to detail due to its reactivity. As an organometallic compound, it is highly sensitive to moisture and air, necessitating inert conditions during storage and reaction setups. This sensitivity underscores the importance of controlled environments in its application, particularly in industrial-scale processes where maintaining stability is paramount.

In recent years, the compound has been explored for its role in the development of novel pharmaceuticals. Its ability to serve as a building block for more complex structures has made it a valuable tool in drug discovery. Specifically, researchers have leveraged its reactivity to introduce complex side chains into molecules, enhancing their pharmacological properties. This has been particularly relevant in the quest for new treatments for various diseases, where structural complexity often correlates with improved efficacy.

One of the most compelling aspects of Magnesium, chloro[(4-chlorophenyl)methyl]- is its role in cross-coupling reactions. These reactions are fundamental to modern synthetic organic chemistry and have enabled the construction of intricate molecular architectures. The compound's ability to participate in such reactions makes it an indispensable reagent for chemists working on the synthesis of natural products and agrochemicals. Furthermore, its use in palladium-catalyzed reactions has opened up new avenues for the development of efficient synthetic routes.

The pharmaceutical industry has also been keenly interested in the potential applications of this compound. Its structural features suggest that it could be modified to create novel therapeutic agents with specific biological activities. For instance, researchers have investigated its use as a precursor for compounds that target neurological disorders. The ability to fine-tune the structure of these molecules through strategic functionalization offers exciting possibilities for future drug development.

From an academic perspective, Magnesium, chloro[(4-chlorophenyl)methyl]- continues to be a subject of intense study. Researchers are exploring new synthetic methodologies that leverage its unique properties while improving safety and efficiency. Advances in catalytic systems have allowed for milder reaction conditions, reducing the environmental impact of processes involving this compound. Such innovations are crucial for sustainable chemistry and align with global efforts to minimize waste and energy consumption.

The compound's versatility extends beyond pharmaceutical applications. It has found utility in materials science, where it contributes to the development of advanced polymers and coatings. Its ability to form stable complexes with other molecules makes it a valuable component in designing materials with tailored properties. This interdisciplinary approach highlights the broad impact of organometallic compounds like Magnesium, chloro[(4-chlorophenyl)methyl]- on various scientific fields.

In conclusion, Magnesium, chloro[(4-chlorophenyl)methyl]- (CAS No. 874-72-6) represents a cornerstone in modern organic synthesis and pharmaceutical research. Its unique chemical properties make it an indispensable tool for chemists seeking to create complex molecules with potential therapeutic applications. As research continues to uncover new uses and improve synthetic techniques, this compound will undoubtedly remain at the forefront of scientific innovation.

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