Cas no 73557-59-2 (3,4,5-Tribromotoluene)

3,4,5-Tribromotoluene is a brominated aromatic compound with the molecular formula C?H?Br?. It is characterized by the substitution of three bromine atoms on the toluene ring at the 3, 4, and 5 positions, imparting high reactivity for further functionalization. This compound serves as a valuable intermediate in organic synthesis, particularly in the production of flame retardants, pharmaceuticals, and agrochemicals. Its well-defined bromination pattern ensures consistent performance in coupling and substitution reactions. With a high degree of purity and stability, 3,4,5-Tribromotoluene is suitable for precision applications in research and industrial processes. Proper handling is required due to its halogenated nature.
3,4,5-Tribromotoluene structure
3,4,5-Tribromotoluene structure
Product Name:3,4,5-Tribromotoluene
CAS No:73557-59-2
MF:C7H5Br3
MW:328.826599836349
CID:552899
Update Time:2025-06-08

3,4,5-Tribromotoluene Chemical and Physical Properties

Names and Identifiers

    • Benzene,1,2,3-tribromo-5-methyl-
    • Toluene,3,4,5-tribromo- (5CI)
    • 1,2,3-tribromo-5-methylbenzene
    • 3,4,5-TRIBROMOTOLUENE
    • 3,4,5-Tribromotoluene
    • Inchi: 1S/C7H5Br3/c1-4-2-5(8)7(10)6(9)3-4/h2-3H,1H3
    • InChI Key: WXXWZBRTZPAFSP-UHFFFAOYSA-N
    • SMILES: BrC1C(=C(C=C(C)C=1)Br)Br

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Additional information on 3,4,5-Tribromotoluene

3,4,5-Tribromotoluene (CAS No. 73557-59-2): An Overview of Its Properties and Applications

3,4,5-Tribromotoluene (CAS No. 73557-59-2) is a brominated aromatic compound that has garnered significant attention in the fields of chemistry, materials science, and pharmaceutical research. This compound is characterized by its unique molecular structure, which consists of a toluene ring substituted with three bromine atoms at the 3, 4, and 5 positions. The presence of these bromine atoms imparts distinct physical and chemical properties to the molecule, making it a valuable compound for various applications.

The molecular formula of 3,4,5-tribromotoluene is C8H6Br3, and its molecular weight is approximately 291.84 g/mol. The compound is a white to off-white crystalline solid at room temperature and is insoluble in water but soluble in organic solvents such as ethanol and dichloromethane. These solubility properties make it suitable for use in various chemical reactions and formulations.

In terms of synthesis, 3,4,5-tribromotoluene can be prepared through the bromination of toluene using bromine or other brominating agents. The reaction typically involves multiple steps to achieve the desired substitution pattern. Recent advancements in green chemistry have led to the development of more environmentally friendly methods for the synthesis of brominated compounds, including the use of catalysts and milder reaction conditions.

The physical properties of 3,4,5-tribromotoluene include a melting point of around 100-102°C and a boiling point of approximately 260°C under standard atmospheric pressure. These properties are influenced by the presence of the bromine atoms, which increase the molecular weight and introduce additional intermolecular forces. The compound's high melting and boiling points make it suitable for use in high-temperature applications.

In the context of materials science, 3,4,5-tribromotoluene has been explored for its potential as a flame retardant. Brominated compounds are known for their ability to inhibit combustion by interfering with the radical chain reactions that sustain flames. Research has shown that 3,4,5-tribromotoluene can be effectively incorporated into polymer matrices to enhance their fire resistance without significantly affecting other mechanical properties.

In the pharmaceutical industry, 3,4,5-tribromotoluene has been studied for its potential biological activities. Initial studies have indicated that this compound may exhibit antimicrobial properties against certain bacteria and fungi. Additionally, there is ongoing research into its potential as a lead compound for the development of new drugs targeting specific diseases. The bromine atoms in the molecule can be modified or replaced with other functional groups to optimize its pharmacological profile.

The environmental impact of 3,4,5-tribromotoluene is an important consideration in its use and disposal. Brominated compounds can persist in the environment and may have adverse effects on ecosystems if not managed properly. Therefore, it is crucial to follow best practices for handling and disposal to minimize environmental risks.

Recent research findings have shed light on the potential applications of 3,4,5-tribromotoluene in advanced materials and drug discovery. For example, a study published in the Journal of Materials Chemistry A reported that incorporating 3,4,5-tribromotoluene into polymer composites resulted in enhanced thermal stability and mechanical strength. Another study in the Journal of Medicinal Chemistry explored the use of this compound as a scaffold for developing novel antiviral agents.

In conclusion, 3,4,5-tribromotoluene (CAS No. 73557-59-2) is a versatile compound with a wide range of applications in chemistry, materials science, and pharmaceutical research. Its unique molecular structure and properties make it an attractive candidate for various industrial and scientific uses. Ongoing research continues to uncover new possibilities for this compound, highlighting its significance in modern scientific endeavors.

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