30609-79-1

Usage

Uses

Used in Polymer and Resin Synthesis:
Phenol,4,4'-sulfonylbis[2,6-dichlorois used as a precursor in the synthesis of various polymers and resins. Its unique structure allows it to act as a building block for the formation of complex polymeric materials with specific properties, such as high thermal stability, mechanical strength, and chemical resistance.
Used in Fungicide Applications:
Phenol,4,4'-sulfonylbis[2,6-dichlorois used as a fungicide to protect crops and other plants from fungal infections. Its chemical properties enable it to inhibit the growth and reproduction of fungi, thereby preventing the spread of diseases and ensuring healthy plant growth.
Used in Bactericide Applications:
In addition to its fungicidal properties, Phenol,4,4'-sulfonylbis[2,6-dichlorois also used as a bactericide. It can effectively kill or inhibit the growth of bacteria, making it useful in various applications such as water treatment, food preservation, and medical disinfection.
Used in Chemical Synthesis:
Phenol,4,4'-sulfonylbis[2,6-dichlorocan be used as an intermediate in the synthesis of other chemical compounds. Its reactive functional groups make it a valuable building block for the production of various organic and inorganic compounds, including pharmaceuticals, dyes, and specialty chemicals.
Used in Research and Development:
Due to its unique structure and properties, Phenol,4,4'-sulfonylbis[2,6-dichlorois often used in research and development for the study of new materials, chemical reactions, and potential applications. It can serve as a model compound for understanding the behavior of bisphenols and their derivatives in various chemical and biological systems.

Upstream product

• 80-09-1 4,4'-sulfonediphenol 

Downstream Products

• 1297592-25-6 C₄H₁₀N₂*C₁₂H₆Cl₄O₄S 

Relevant academic research and scientific papers

Organic complexes built by halogenated molecules: Unexpected in situ C-N bond formation in metal-free solvothermal conditions

Reactions of two halogenated derivatives of bis(4-hydroxyphenyl)sulphone (BPS, 1), tetrabromobisphenol-S (TBBPS, 2), and tetrachlorobisphenol-S (TCBPS, 3), with piperazine (PZ, 4), were investigated by means of the combinational usage of solvothermal and mechanochemical methods. The resultant organic complexes, [(C6H2OBr2)2SO 2]?[(C4H10N2) 2CH2] (5), [(C6H2OBr 2)2SO2]2?(C4H 12N2)2?3(CH3OH) (6), [(C 6H2OCl2)2SO2] ?[(C4H10N2)2CH2] (7), and [(C6H2OCl2)2SO 2]2?(C4H12N2) 2?3(CH3OH) (8), were fully characterized by single crystal and powder X-ray diffractions. In the cases of complexes 5 and 7 that were prepared from solvothermal conditions, a rare metal-free in situ ligand formation has been observed, in which the new organic molecule 1,2-bispiperazinylmethane was presumably originated from the double C-N coupling of two piperazines on a carbon atom coming from methanol. In addition, the relevant concomitants 6 and 8 were also isolated from the solutions of 5 and 7, respectively. Complexes 6 and 8 contain 1:1 starting molecules of 2/3 with 4 assembled into helical structures.