7205-72-3

Usage

Uses

Used in Pharmaceutical Research:
(4-chlorophenyl) isopropyl sulfoxide is used as a precursor in the synthesis of new drug compounds, contributing to the advancement of medicinal chemistry.
Used in Central Nervous System Disorders:
In the pharmaceutical industry, (4-chlorophenyl) isopropyl sulfoxide is used as a potential serotonin receptor agonist for the development of drugs targeting central nervous system disorders.
Used in Antioxidant and Anti-Inflammatory Applications:
(4-chlorophenyl) isopropyl sulfoxide is also utilized in the research and development of drugs with potential antioxidant and anti-inflammatory properties, further expanding its applications in medicinal chemistry and drug development.

Upstream product

• 7205-62-1 1-chloro-4-(isopropylthio)benzene 
• 3085-42-5 bis(4-chlorophenyl)sulfoxide 
• 108-90-7 chlorobenzene 

Downstream Products

• 55698-07-2 1-Chloro-4-(2-chloro-propane-2-sulfinyl)-benzene 

Relevant academic research and scientific papers

Desymmetrization of prochiral diaryl sulfoxides by an asymmetric sulfoxide-magnesium exchange

The first desymmetrizations of prochiral diaryl sulfoxides 1 by an asymmetric sulfoxide-magnesium exchange reaction are reported. The respective substrate (1), iPr2Mg, and the dilithium salt of (S)-BINOL (which was prepared in situ) provided (S)-configured aryl isopropyl sulfoxides 2 in up to 91 % yield and with up to 91 % ee. (S)-BINOL was re-isolable in 98 % yield. Copyright

Selective aerobic oxidation of sulfides to sulfoxides catalyzed by coenzyme NAD+ models

Coenzyme NAD+ models can be applied in the photooxygenation of sulfides to sulfoxides as organocatalysts at room temperature. A series of sulfoxides are synthesized easily with this protocol and the possible mechanism is discussed. This procedure provides a reliable approach to the clean production of useful sulfoxides in synthetic chemistry.

ELECTRONIC EFFECTS IN ALKYL 4-CHLOROPHENYL SULFONE AND SULFOXIDE MOLECULES ACCORDING TO 35Cl NQR DATA

Compounds of the 4-ClC6H4S(O)CHn.(CH3)3-n and 4-ClC6H4SO2R series nH and CHn(CH3)3-n> were synthesized and studied by the 35Cl NQR method.It was found that their NQR frequencies change regularly with increase in the number n.