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AE08090

10570-67-9 | 2,6-Dimethyl-4-iodophenol

Packsize Purity Availability Price Discounted Price    Quantity
1g 97% in stock $15.00 $10.00 -   +
5g 97% in stock $18.00 $12.00 -   +
25g 97% in stock $21.00 $15.00 -   +

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Description
Catalog Number: AE08090
Chemical Name: 2,6-Dimethyl-4-iodophenol
CAS Number: 10570-67-9
Molecular Formula: C8H9IO
Molecular Weight: 248.0609
MDL Number: MFCD00094415
SMILES: Ic1cc(C)c(c(c1)C)O

 

Computed Properties
Complexity: 104  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 10  
Hydrogen Bond Acceptor Count: 1  
Hydrogen Bond Donor Count: 1  
XLogP3: 2.9  

 

 

Upstream Synthesis Route 
  • 4-Iodo-2,6-dimethylphenol, also known as $name$, is a versatile compound widely utilized in chemical synthesis for its unique reactivity and functional properties. In the realm of organic chemistry, this compound serves as a key building block for the synthesis of various pharmaceuticals, agrochemicals, and materials.One of the main applications of 4-Iodo-2,6-dimethylphenol in chemical synthesis is its role as a reagent in the formation of carbon-carbon and carbon-heteroatom bonds. The iodo group on the aromatic ring can undergo various substitution reactions, enabling the introduction of different functional groups. This versatility makes it a valuable tool in designing and creating complex organic molecules.Furthermore, the dimethylphenol moiety provides steric hindrance and electronic effects that can influence the regioselectivity and reactivity of the compound in certain reactions. This property is particularly useful in controlling the outcome of diverse chemical transformations, such as electrophilic aromatic substitutions or nucleophilic additions.Overall, by leveraging the properties of 4-Iodo-2,6-dimethylphenol, chemists can efficiently access a wide range of structurally diverse compounds, making it an indispensable component in modern chemical synthesis strategies.
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