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1-(4-hydroxy-3-methoxyphenyl)-3-p-tolylpropan-2-one is used as a fine chemical.
1-(4-hydroxy-3-methoxyphenyl)-3-p-tolylpropan-2-one is a specialized diaryl ketone intermediate combining vanillyl and p-tolyl structural motifs. Primarily valued in fine chemical synthesis, it serves as a versatile building block for developing novel pharmaceuticals and niche fragrance compounds. Its key selling points include unique structural diversity, enabling chemists to explore new structure-activity relationships in drug discovery, particularly for bioactive molecules requiring specific aromatic substitutions. In perfumery, it offers potential for creating distinctive warm, spicy-woody notes unavailable from standard vanilla derivatives. The molecule’s reactive ketone center and phenolic hydroxyl group provide excellent derivatization flexibility, allowing precise tuning of solubility and reactivity for custom R&D applications. Ideal for laboratories seeking high-purity, non-commodity intermediates, it supports innovation in creating proprietary scent profiles or targeted therapeutic candidates where standard bulk chemicals fall short.
| Product Name | 1-(4-hydroxy-3-methoxyphenyl)-3-p-tolylpropan-2-one |
| Apperance | White powder |
| EINECS | N/A |
| MF | C17H18O3 |
| MW | 270.32 |
| Assay | ≥99.0% |
| Product parameters | |
| Cas number: | 134612-39-8 |
| Appearance: | White powder |
| Purity: | 99.0%min |
| Package details: | 1kg/foil bag, 25kg/drum or as you require |
| Brand: | Fortunachem |
1-(4-hydroxy-3-methoxyphenyl)-3-p-tolylpropan-2-one is a synthetic organic compound belonging to the class of diaryl ketones (specifically, a substituted phenylacetone derivative). Structurally, it combines a vanillyl group (4-hydroxy-3-methoxyphenyl, derived from vanillin) and a p-tolyl group (4-methylphenyl) linked by a three-carbon ketone backbone.
It is primarily used as a specialty intermediate in fine chemical synthesis and fragrance research. Unlike common industrial solvents or bulk chemicals, this molecule is valued for its specific structural features which allow it to serve as a precursor for more complex bioactive molecules or custom scent profiles.
Key Selling Points
Unique Fragrance Profile Potential:
The combination of the vanilla-like vanillyl moiety and the aromatic p-tolyl group suggests potential applications in niche perfumery. It may offer warm, spicy, or woody-floral notes distinct from standard vanillin derivatives, appealing to fragrance houses seeking novel olfactory ingredients for luxury scents.
Versatile Synthetic Intermediate:
The ketone functionality and the activated aromatic rings make it an excellent building block for medicinal chemistry. It can be readily modified (e.g., via reductive amination, aldol condensation, or ring closure) to synthesize potential pharmaceutical candidates, particularly those targeting receptors influenced by styryl or diarylalkane structures.
Customization for R&D:
As a non-commodity chemical, its primary market is research and development. Laboratories purchasing this compound value it for structure-activity relationship (SAR) studies, where the specific placement of the hydroxyl, methoxy, and methyl groups allows scientists to probe biological activity or material properties with high precision.
Derivatization Flexibility:
The phenolic hydroxyl group allows for easy etherification or esterification, enabling chemists to tune the molecule's solubility, stability, and reactivity for specific downstream applications, such as creating prodrugs or polymer additives.
Note: This is a specialized fine chemical. It is not a mass-market commodity like cellulase or α -cyclodextrin, and its "selling points" are targeted specifically at synthetic chemists and fragrance developers rather than general industrial manufacturers.
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