3937-99-3

Usage

Uses

Used in Pharmaceutical Industry:
AKOS BBS-00002841 is used as a building block for the synthesis of various pharmaceuticals and organic compounds, due to its unique molecular structure that may contribute to the development of new drugs and therapeutic agents.
Used in Medicinal Chemistry:
AKOS BBS-00002841 is used as a precursor in medicinal chemistry for the exploration of its potential applications in the discovery and design of novel pharmaceuticals, given its chemical composition and the possibility of its involvement in the synthesis of bioactive molecules.
Note: Since there are no specific applications mentioned in the provided materials, the uses listed above are inferred based on the potential of AKOS BBS-00002841 as a building block and precursor in the pharmaceutical and medicinal chemistry industries. Further research would be necessary to validate these potential uses.

Upstream product

• 6140-09-6 sodium 4-methoxy-benzenesulfonate 
• 79-11-8 chloroacetic acid 
• 696-63-9 4-Methoxybenzenethiol 
• 3406-77-7 (4-methoxy-phenylsulfanyl)-acetic acid 
• 3996-45-0 p-OMeC6H4SOCH2COOH 

Downstream Products

• 53848-52-5 methyl 2-((4-methoxyphenyl)sulfonyl)acetate 
• 76859-80-8 (E)-1-(2-((4-methoxyphenyl)sulfonyl)vinyl)-2-chlorobenzene 
• 76859-82-0 (E)-1-(2-((4-methoxyphenyl)sulfonyl)vinyl)-4-methoxybenzene 
• 68668-00-8 (E)‐1‐methoxy‐4‐(styrylsulfonyl)benzene 
• 1538-95-0 1-((diazomethyl)sulfonyl)-4-methoxybenzene 
• 41024-54-8 2-(4-methoxyphenylsulfonyl)-1-phenylethanone 
• 76859-81-9 (E)-1-(2-((4-methoxyphenyl)sulfonyl)vinyl)-4-chlorobenzene 
• 29312-03-6 4-Methoxyphenyl-dijodmethyl-sulfon 

Relevant academic research and scientific papers

Synthesis and antioxidant activity of bis unsaturated sulfones, bis pyrroles, and bis pyrazoles

The Michael acceptor 1,4-bis-(E)-2-(arylsulfonylvinyl)benzene was exploited to prepare a new series of bis heterocycles-(1,4-phenylene)bis(arylsulfonylpyrrole) and (1,4-phenylene)bis(arylsulfonyl pyrazole). All of the compounds were tested for antioxidant activity. Amongst the tested compounds, 1,4-bis-(E)-2-(arylsulfonylvinyl)benzene (5) was found to be the best potential antioxidant agent.

Mass spectra of arylsulphonylacetic acids and correlation of fragment ions with substituent constants

The mass spectral studies of arylsulphonylacetic acids reveal that the skeletal rearrangement via aryl-oxygen bond formation is predominant with a weak competing alkyl migration.A linear correlation is obtained between the intensities of + ions, i.e. +> and the Hammett substituent constants.

SYNTHESIS AND SPECTRAL STUDIES OF SOME UNSATURATED SULPHONES

A new 5-chloro-2-methylbenzenesulphonylacetic acid has been prepared from 4-chlorotoluene.The condensation of this acid and 4-bromo, 4-methoxy, 3,4-dichloro and 4-chloro-3-methylbenzenesulphonylacetic acid with different araldehydes gave some new unsatura