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7402-69-9

4-(benzenesulfonyl)phenol

Catalog#: AR0037D2  |   CAS#: 7402-69-9  |   MDL#: MFCD00025037  |   MF: C12H10O3S  |   MW: 234.271

Packsize Purity Price Availability Quantity
50mg 95% $116.00 2-3 weeks Buy Now Add To Cart
100mg 95% $160.00 2-3 weeks Buy Now Add To Cart
250mg 95% $221.00 2-3 weeks Buy Now Add To Cart
500mg 95% $398.00 2-3 weeks Buy Now Add To Cart
1g 95% $536.00 2-3 weeks Buy Now Add To Cart
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Catalog Number AR0037D2
Chemical Name 4-(benzenesulfonyl)phenol
CAS Number 7402-69-9
Molecular Formula C12H10O3S
Molecular Weight 234.271
MDL Number MFCD00025037
SMILES Oc1ccc(cc1)S(=O)(=O)c1ccccc1
NSC Number 400311

4-(Benzenesulfonyl)phenol, a versatile compound used in chemical synthesis, plays a crucial role in various reactions due to its unique properties. With its aromatic ring and sulfonyl functional group, this compound serves as an important building block for the synthesis of pharmaceuticals, agrochemicals, and materials.In organic synthesis, 4-(benzenesulfonyl)phenol is commonly employed as a protecting group for alcohols. By selectively masking hydroxyl groups with the benzenesulfonyl moiety, this compound allows for controlled reactions without affecting other reactive groups in a molecule. This protection-deprotection strategy is essential in the synthesis of complex organic molecules, ensuring the desired functionality is preserved throughout the synthetic pathway.Furthermore, 4-(benzenesulfonyl)phenol is utilized in the preparation of aryl sulfonates, which are important intermediates in various chemical transformations. The sulfonyl group can act as a directing or activating group in transition metal-catalyzed cross-coupling reactions, facilitating the formation of carbon-carbon and carbon-heteroatom bonds. This enables the efficient construction of aryl-aryl, aryl-heteroaryl, and aryl-alkyl linkages, expanding the synthetic toolbox for chemists in designing novel compounds.Additionally, the presence of the benzenesulfonyl group in 4-(benzenesulfonyl)phenol imparts stability and solubility to the compound, making it compatible with a wide range of reaction conditions. This versatility allows for its incorporation into diverse synthetic strategies, enhancing the efficiency and selectivity of chemical transformations.Overall, 4-(benzenesulfonyl)phenol is a valuable reagent in chemical synthesis, enabling precise control over functional group manipulations and facilitating the construction of complex molecular architectures. Its applications extend across various fields of organic chemistry, making it an indispensable tool for synthetic chemists seeking to develop new compounds with tailored properties.
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