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53755-58-1

2-Propenoic acid, 3-[4-hydroxy-3-(3-methyl-2-buten-1-yl)phenyl]-, (2E)-

Catalog#: AR01SH8P  |   CAS#: 53755-58-1  |   MDL#:  |   MF: C14H16O3  |   MW: 232.2750

Packsize Purity Price Availability Quantity
1mg 98% $210.00 Global Stock Buy Now Add To Cart
5mg 98% $462.00 Global Stock Buy Now Add To Cart
10mg 98% $739.00 Global Stock Buy Now Add To Cart
25mg 98% $1,477.00 Global Stock Buy Now Add To Cart
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Catalog Number AR01SH8P
Chemical Name 2-Propenoic acid, 3-[4-hydroxy-3-(3-methyl-2-buten-1-yl)phenyl]-, (2E)-
CAS Number 53755-58-1
Molecular Formula C14H16O3
Molecular Weight 232.2750
SMILES CC(=CCc1cc(/C=C/C(=O)O)ccc1O)C

Drupanin, a powerful and versatile reagent, is widely used in chemical synthesis for various applications. Its unique composition and properties make it a valuable tool for synthetic organic chemists.In the realm of organic synthesis, Drupanin serves as a key component for the oxidation of alcohols to carbonyl compounds. With its ability to efficiently convert primary alcohols to aldehydes and secondary alcohols to ketones, Drupanin plays a crucial role in the formation of these important functional groups.Furthermore, Drupanin is instrumental in the synthesis of heterocyclic compounds, where its oxidative capabilities facilitate the construction of complex ring structures. By enabling the formation of key intermediates in heterocycle synthesis, Drupanin allows chemists to access a wide range of biologically active molecules and pharmaceuticals.Beyond its applications in alcohol oxidation and heterocycle synthesis, Drupanin also finds utility in the functionalization of aromatic compounds. Through selective oxidation reactions, Drupanin enables the introduction of diverse functional groups onto aromatic rings, expanding the scope of synthetic possibilities in organic chemistry.Overall, Drupanin stands out as a versatile and indispensable reagent in chemical synthesis, offering chemists a powerful tool for the efficient construction of complex molecules and the exploration of new synthetic pathways.
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