o-Iodotoluene

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Identification

Molecular formula
C7H7I
CAS Number
615-37-2
IUPAC Name
1-iodo-2-methyl-benzene
Molecular Weight
202.04g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.6570g/cm3
Synonyms
2-Iodotoluene
Interesting facts

Interesting Facts about 1-Iodo-2-methyl-benzene

1-Iodo-2-methyl-benzene, also known as orthoiodobenzene or o-iodotoluene, is a fascinating compound that offers a variety of interesting applications and properties. Here are some compelling points about this aromatic halide:

  • It belongs to the class of organic compounds known as iodobenzenes, which are characterized by the presence of iodine atoms bonded to a benzene ring. This functional group significantly influences the reactivity and physical properties of the compound.
  • The compound is often utilized in synthetic organic chemistry as a building block for the formation of larger, more complex molecules. Its iodine substituent enables nucleophilic substitution reactions, making it valuable for developing various chemicals.
  • In the realm of pharmaceuticals, 1-iodo-2-methyl-benzene is investigated for its potential in drug synthesis. Many medicinal compounds include iodine due to its unique biological properties, including potential antiseptic effects and roles in metabolism.
  • It can serve as a precursor for the generation of biologically active compounds, further showcasing its versatility in chemical research.

As noted in chemical literature, “The unique characteristics of halogenated compounds like 1-iodo-2-methyl-benzene open pathways to innovative discoveries in material science and medicinal chemistry.” This highlights the importance of studying such compounds in understanding broader themes in chemistry.

Furthermore, being a derivative of toluene, this compound represents the relationship between simple aromatic hydrocarbons and their halogenated forms, emphasizing the subtle changes in properties induced by halogenation. Researchers continue to explore its potential applications and the mechanisms of its reactivity.

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