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5325-04-2

4′-Hydroxy-3′,5′-dimethylacetophenone

Catalog#: AR003LAR  |   CAS#: 5325-04-2  |   MDL#: MFCD00195574  |   MF: C10H12O2  |   MW: 164.2011

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100mg 97% $21.00 Global Stock Buy Now Add To Cart
1g 97% $23.00 Global Stock Buy Now Add To Cart
5g 97% $73.00 Global Stock Buy Now Add To Cart
10g 97% $140.00 Global Stock Buy Now Add To Cart
25g 97% $222.00 Global Stock Buy Now Add To Cart
100g 97% $885.00 Global Stock Buy Now Add To Cart
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Catalog Number AR003LAR
Chemical Name 4′-Hydroxy-3′,5′-dimethylacetophenone
CAS Number 5325-04-2
Molecular Formula C10H12O2
Molecular Weight 164.2011
MDL Number MFCD00195574
SMILES CC(=O)c1cc(C)c(c(c1)C)O
NSC Number 109 

3,5-Dimethyl-4-hydroxyacetophenone, also known as $name$, is a versatile compound widely utilized in chemical synthesis. With its unique structure and properties, this compound finds key applications in various organic reactions and transformations.In the realm of chemical synthesis, $name$ serves as a valuable building block for the synthesis of advanced pharmaceutical intermediates and specialty chemicals. Its functional groups enable it to participate in a range of reactions, including Friedel-Crafts acylation, alkylation, and cyclization reactions. Moreover, $name$ is frequently employed as a key starting material for the synthesis of complex natural products and biologically active molecules. Its strategic placement of methyl and hydroxy groups provides opportunities for selective functionalization, enabling chemists to tailor the molecule for specific target compounds.Furthermore, due to its structural versatility, $name$ is utilized in the synthesis of materials with potential applications in organic electronics, such as OLEDs (organic light-emitting diodes) and optoelectronic devices. Its robust chemical reactivity and compatibility with various synthetic methods make it a valuable tool for designing and constructing novel functional materials.In summary, the application of 3,5-Dimethyl-4-hydroxyacetophenone in chemical synthesis spans diverse areas, ranging from pharmaceutical chemistry to materials science. Its role as a key intermediate and building block underscores its importance in modern organic synthesis practices, enabling the creation of complex molecules and materials with tailored properties and functionalities.
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