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3-Iodotoluene CAS:625-95-6

3-Iodotoluene is an organic compound with the molecular formula C8H9I, characterized by an iodine atom situated at the meta position relative to a methyl group on a benzene ring. This halogenated aromatic compound is significant in organic synthesis due to its unique reactivity and ability to serve as a versatile intermediate. The presence of iodine enhances the electrophilic nature of the aromatic system, facilitating various nucleophilic substitution reactions. 3-Iodotoluene finds applications in pharmaceuticals, agrochemicals, and material science, where it can be transformed into a range of biologically active compounds and functionalized materials.


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Application and Effect:

3-Iodotoluene, also known as meta-iodotoluene, is a member of the iodinated aromatic hydrocarbon family. Its structure features a methyl group and an iodine atom attached to a benzene ring, imparting distinct chemical properties that are highly relevant in synthetic organic chemistry. The introduction of the iodine substituent enhances the electrophilicity of the aromatic ring, making it a valuable substrate for various chemical transformations. One of the primary uses of 3-iodotoluene lies in its role as an intermediate in the pharmaceutical industry. It can be utilized to synthesize a variety of bioactive compounds through nucleophilic substitution reactions, where the iodine can be replaced by different nucleophiles such as amines, alcohols, or thiols. These modifications enable the development of novel therapeutic agents with potential applications in treating various diseases, including cancer and inflammation. Additionally, 3-iodotoluene can participate in cross-coupling reactions, such as the Suzuki, Heck, or Sonogashira reactions. These methodologies allow for the formation of carbon-carbon bonds, enabling chemists to construct complex molecular frameworks often required in drug design and development. The iodo group acts as an efficient leaving group in these reactions, promoting the coupling process with alkyl or aryl groups. In materials science, 3-iodotoluene serves as a precursor for synthesizing functionalized polymers and nanomaterials. Its reactive nature facilitates the incorporation of various functional groups, allowing researchers to tailor the physical and chemical properties of materials for specific applications, such as electronics, sensors, and coatings. Moreover, 3-iodotoluene is beneficial in research settings, particularly in studying the mechanisms of electrophilic aromatic substitution and other fundamental organic reactions. Its predictable reactivity profiles make it a reliable model compound for exploring new synthetic pathways. Another important application of 3-iodotoluene is in the field of dye and pigment synthesis, where it can be employed to create colorants with enhanced stability and functionality. In summary, 3-iodotoluene is a multifaceted compound with significant implications in organic synthesis, medicinal chemistry, and materials science. Its unique structural properties and reactivity make it an essential building block for developing diverse chemical entities, driving ongoing research aimed at uncovering new applications and methodologies. As advancements continue in synthetic strategies, 3-iodotoluene remains a key compound in the quest for innovative solutions in both academic and industrial contexts.

Product Sample:

L-Arginine1
L-Arginine2

Product Packing:

L-Arginin3

Additional Information:

Composition C7H7I
Assay 99%
Appearance white powder
CAS No.  625-95-6
Packing Small and bulk
Shelf Life 2 years
Storage Store in cool and dry area
Certification ISO.

 


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