Cas no 29875-06-7 (Magnesium,chloro[(3-methylphenyl)methyl]-)

Magnesium, chloro[(3-methylphenyl)methyl]-, is an organomagnesium compound commonly utilized as a Grignard reagent in organic synthesis. Its key advantages include high reactivity in carbon-carbon bond-forming reactions, making it valuable for the preparation of complex organic molecules. The presence of the 3-methylphenyl group enhances its stability and selectivity in nucleophilic additions to carbonyl compounds, ketones, and esters. This reagent is particularly effective in anhydrous conditions, ensuring consistent performance in sensitive reactions. Its compatibility with a range of solvents, such as THF and diethyl ether, further broadens its applicability in synthetic chemistry. Proper handling under inert atmospheres is recommended to maintain its efficacy.
Magnesium,chloro[(3-methylphenyl)methyl]- structure
29875-06-7 structure
Product Name:Magnesium,chloro[(3-methylphenyl)methyl]-
CAS No:29875-06-7
MF:C8H9ClMg
MW:164.915061712265
MDL:MFCD01319905
CID:240573
PubChem ID:24880010
Update Time:2025-06-08

Magnesium,chloro[(3-methylphenyl)methyl]- Chemical and Physical Properties

Names and Identifiers

    • Magnesium,chloro[(3-methylphenyl)methyl]-
    • 3-Methylbenzylmagnesium chloride
    • 3-Methylbenzylmagnesium chloride, 0.25 M solution in THF, SpcSeal
    • 3-Methylbenzylmagnesiumchloride,0.25MsolutioninTHF,inresealablebottle
    • magnesium,1-methanidyl-3-methylbenzene,chloride
    • 3-methyl-benzyl magnesium chloride
    • 3-Methylbenzylmagnesium chloride 0.25 M in Tetrahydrofuran
    • 3-Methylbenzylmagnesium chloride solution
    • 3-MethylbenzylMagnesiuM chloride, 0.25M in 2-MeTHF
    • 3-Methylbenzylmagnesium chloride, 0.25M solution in THF, AcroSeal
    • m-CH3C6H4CH2MgCl
    • m-methylbenzylmagnesium chloride
    • m-Methyl-benzylmagnesiumchlorid
    • m-xylylmagnesium chloride
    • Chloro(m-methylbenzyl)magnesium
    • MDL: MFCD01319905
    • Inchi: 1S/C8H9.ClH.Mg/c1-7-4-3-5-8(2)6-7;;/h3-6H,1H2,2H3;1H;/q-1;;+2/p-1
    • InChI Key: MPIXEEVXDGICED-UHFFFAOYSA-M
    • SMILES: [Cl-].[Mg+2].C1([CH2-])C=CC=C(C)C=1

Computed Properties

  • Exact Mass: 164.02400
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 0
  • Heavy Atom Count: 10
  • Rotatable Bond Count: 0
  • Complexity: 75.7
  • 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
  • Surface Charge: 0
  • Tautomer Count: nothing
  • XLogP3: nothing

Experimental Properties

  • Color/Form: Tawny liquid
  • Density: 0.923?g/mL?at 25?°C
  • Boiling Point: 65?°C
  • Flash Point: Degrees Fahrenheit:<1.4°F
    Degrees Celsius:<-17°C
  • PSA: 0.00000
  • LogP: 3.00020
  • Color/Form: 0.5?M in THF
  • Solubility: Not available

Magnesium,chloro[(3-methylphenyl)methyl]- Security Information

Magnesium,chloro[(3-methylphenyl)methyl]- Customs Data

  • HS CODE:29310099

Magnesium,chloro[(3-methylphenyl)methyl]- Pricemore >>

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Magnesium,chloro[(3-methylphenyl)methyl]- Suppliers

Amadis Chemical Company Limited
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(CAS:29875-06-7)Magnesium,chloro[(3-methylphenyl)methyl]-
Order Number:A1209723
Stock Status:in Stock
Quantity:250ml/100ml
Purity:99%
Pricing Information Last Updated:Friday, 30 August 2024 03:53
Price ($):1509.0/943.0

Additional information on Magnesium,chloro[(3-methylphenyl)methyl]-

Magnesium,chloro[(3-methylphenyl)methyl]- (CAS No. 29875-06-7): A Comprehensive Overview in Modern Chemical Research

Magnesium,chloro[(3-methylphenyl)methyl]-, identified by its Chemical Abstracts Service (CAS) number 29875-06-7, is a significant compound in the realm of organometallic chemistry and pharmaceutical research. This organomagnesium reagent, characterized by its chloro-substituted structure and the presence of a 3-methylphenyl group, has garnered considerable attention due to its versatile applications in synthetic chemistry and medicinal chemistry.

The compound's molecular structure, featuring a magnesium center coordinated to a chloro ligand and an 3-methylphenylmethyl group, imparts unique reactivity that makes it invaluable in various synthetic transformations. Its ability to participate in Grignard reactions, cross-coupling reactions, and as a precursor in the synthesis of more complex molecules has positioned it as a cornerstone in modern chemical synthesis.

In recent years, the applications of Magnesium,chloro[(3-methylphenyl)methyl]- have expanded into the pharmaceutical industry. Researchers have leveraged its reactivity to develop novel drug candidates and intermediates. For instance, its role in constructing complex organic frameworks has been instrumental in the synthesis of biologically active molecules. The compound's ability to facilitate the formation of carbon-carbon bonds has made it particularly useful in the development of therapeutic agents targeting various diseases.

One of the most compelling aspects of Magnesium,chloro[(3-methylphenyl)methyl]- is its utility in asymmetric synthesis. The presence of the chiral 3-methylphenyl group allows for the selective formation of enantiomerically pure compounds, which are crucial in pharmaceuticals where stereochemistry often dictates efficacy and safety. Recent studies have demonstrated its effectiveness in generating enantiomerically enriched products, paving the way for more efficient and sustainable drug development processes.

The compound's stability under various reaction conditions has also been a subject of extensive research. Studies have shown that Magnesium,chloro[(3-methylphenyl)methyl]- can be stored and handled under inert atmospheres without significant degradation, making it a reliable reagent for large-scale syntheses. This stability is particularly important in industrial settings where reproducibility and cost-effectiveness are paramount.

In addition to its synthetic applications, Magnesium,chloro[(3-methylphenyl)methyl]- has shown promise in material science. Its ability to form coordination complexes with various ligands has led to the development of novel materials with unique properties. These materials have potential applications in catalysis, sensors, and even nanotechnology. The compound's versatility underscores its importance not just as a synthetic tool but as a building block for innovative materials.

The role of organomagnesium compounds like Magnesium,chloro[(3-methylphenyl)methyl]- in drug discovery continues to evolve with advancements in chemical biology and computational chemistry. Researchers are increasingly using computational methods to predict the reactivity and behavior of these compounds, enabling more targeted and efficient synthetic strategies. This integration of computational tools with traditional wet chemistry has significantly accelerated the pace of drug development.

The environmental impact of using organomagnesium reagents such as Magnesium,chloro[(3-methylphenyl)methyl]- is also a critical consideration. Efforts are underway to develop greener synthetic methodologies that minimize waste and reduce energy consumption. Innovations such as flow chemistry and biocatalysis are being explored to make the use of these reagents more sustainable. These advancements not only benefit the environment but also enhance the economic viability of pharmaceutical manufacturing processes.

The future prospects for Magnesium,chloro[(3-methylphenyl)methyl]- are bright, with ongoing research uncovering new applications and refining existing ones. As our understanding of chemical reactivity continues to deepen, it is likely that this compound will play an even greater role in both academic research and industrial applications. Its unique properties make it indispensable for chemists working at the forefront of synthetic organic chemistry and pharmaceutical science.

Recommended suppliers
Amadis Chemical Company Limited
(CAS:29875-06-7)Magnesium,chloro[(3-methylphenyl)methyl]-
A1209723
Purity:99%/99%
Quantity:250ml/100ml
Price ($):1509.0/943.0
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