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Home  > 2-Chloro-1-iodo-4-methylbenzene

AA16543

116632-42-9 | 2-Chloro-1-iodo-4-methylbenzene

Packsize Purity Availability Price Discounted Price    Quantity
5g 98% in stock $11.00 $8.00 -   +
25g 98% in stock $26.00 $19.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AA16543
Chemical Name: 2-Chloro-1-iodo-4-methylbenzene
CAS Number: 116632-42-9
Molecular Formula: C7H6ClI
Molecular Weight: 252.48000999999996
MDL Number: MFCD00079734
SMILES: Cc1ccc(c(c1)Cl)I

 

Computed Properties
Complexity: 94.9  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 9  
XLogP3: 3.6  

 

 

Upstream Synthesis Route
  • 3-Chloro-4-iodotoluene is a versatile chemical compound that finds wide application in various chemical synthesis processes. When utilized in organic chemistry reactions, this compound serves as a valuable building block for the synthesis of more complex molecules. Its unique structure, containing both chlorine and iodine atoms attached to a toluene backbone, facilitates the creation of diverse chemical structures with specific properties.In chemical synthesis, 3-Chloro-4-iodotoluene can be employed as a key intermediate in the production of pharmaceuticals, agrochemicals, and advanced materials. Its functional groups enable selective reactions that lead to the formation of new carbon-carbon or carbon-heteroatom bonds, crucial for constructing intricate molecular frameworks. By undergoing various transformations such as substitution, elimination, or coupling reactions, this compound plays a crucial role in the creation of novel compounds with tailored functionalities.Furthermore, 3-Chloro-4-iodotoluene is often utilized in cross-coupling reactions, where it serves as a valuable starting material for the synthesis of biaryl compounds. These biaryl structures are prevalent in pharmaceuticals, natural products, and materials science, making this compound an essential building block in the organic chemist's toolkit. Its ability to participate in diverse chemical transformations highlights its significance in the realm of chemical synthesis, where precise control over molecular structure is paramount.
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