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76425-88-2

trans-3-Hydroxystilbene

Catalog#: AR00GH3H  |   CAS#: 76425-88-2  |   MDL#: MFCD00016459  |   MF: C14H12O  |   MW: 196.2445

Packsize Purity Price Availability Quantity
100mg 95% $41.00 Global Stock Buy Now Add To Cart
250mg 95% $70.00 Global Stock Buy Now Add To Cart
1g 95% $188.00 Global Stock Buy Now Add To Cart
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Catalog Number AR00GH3H
Chemical Name trans-3-Hydroxystilbene
CAS Number 76425-88-2
Molecular Formula C14H12O
Molecular Weight 196.2445
MDL Number MFCD00016459
SMILES Oc1cccc(c1)C=Cc1ccccc1

3-Styrylphenol, also known as 1-hydroxy-4-(E)-phenylbuta-1,3-diene, serves as a versatile compound in chemical synthesis. This valuable building block is commonly utilized in organic chemistry for the synthesis of various pharmaceuticals, agrochemicals, and fine chemicals. 3-Styrylphenol's unique structure, characterized by a hydroxyl group and a styryl moiety, imparts distinct reactivity and functional properties that make it an essential intermediate in the preparation of diverse compounds.One prominent application of 3-Styrylphenol is its involvement in the synthesis of biologically active molecules. Its hydroxyl group can undergo different chemical transformations, such as esterification, etherification, or oxidation, leading to the formation of drug candidates, natural product derivatives, or bioactive substances. Furthermore, the conjugated double bond in the styryl group enables key carbon-carbon bond formations via cross-coupling reactions or cyclization processes, allowing for the efficient assembly of complex molecular frameworks.Additionally, 3-Styrylphenol finds utility in the development of advanced materials and functional polymers. By incorporating this compound into polymerization reactions, researchers can introduce specific functionalities, such as UV-absorbing groups, thermoresponsive units, or fluorescent tags, thereby tailoring the properties of the resulting polymers for various applications in optoelectronics, sensors, or biomedical devices.Moreover, 3-Styrylphenol's role in chemical synthesis extends to the creation of specialty chemicals and fine fragrances. Its aromatic structure and reactive functional groups enable the design of novel flavors, perfumes, or additives used in the fragrance industry. Through strategic modifications and derivatization steps, chemists can access a wide array of structurally diverse compounds with unique sensory characteristics and commercial potential.
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GHS Pictogram N/A
UN# -
Hazard Statements -
Class -
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