88-49-3

Usage

Uses

Used in Organic Synthesis:
4-Chloro-2,5-Dimethylbenzenesulfonyl Chloride is used as an intermediate in the synthesis of various complex organic compounds. Its unique structure and reactivity make it a valuable component in the creation of a wide range of chemical products.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4-Chloro-2,5-Dimethylbenzenesulfonyl Chloride is used as a building block for the development of new drugs. Its chemical properties allow it to be incorporated into the molecular structures of potential therapeutic agents, contributing to their overall effectiveness and function.
Used in Chemical Research:
4-Chloro-2,5-Dimethylbenzenesulfonyl Chloride is also utilized in chemical research for studying the properties and reactions of sulfonyl chlorides. Its stability and reactivity provide valuable insights into the behavior of similar compounds, aiding in the advancement of chemical knowledge and the development of new applications.
Used in Specialty Chemicals Production:
In the production of specialty chemicals, 4-Chloro-2,5-Dimethylbenzenesulfonyl Chloride is employed as a key component in the synthesis of specific compounds with unique properties. Its versatility and reactivity make it suitable for creating tailored chemical products for various applications, such as dyes, fragrances, and other specialty materials.

InChI:InChI=1/C8H8Cl2O2S/c1-5-4-8(13(10,11)12)6(2)3-7(5)9/h3-4H,1-2H3

Upstream product

• 95-72-7 2-chloro-1,4-dimethyl-benzene 
• 27897-08-1 4-Amino-2,5-dimethylbenzenesulfonic Acid 

Downstream Products

• 88519-70-4 bis-(4-chloro-2,5-dimethyl-phenyl)-disulfide 
• 609846-56-2 [(S)-4-(4-chloro-2,5-dimethyl-benzenesulfonylamino)-3-oxo-morpholin-2-yl]-acetic acid methyl ester 
• 873589-04-9 N-tert-butyl-2,5-dimethyl-4-chlorobenzenesulfonamide 
• 1011478-03-7 3'-(4-chloro-2,5-dimethyl-benzenesulfonylamino)-2'-methyl-biphenyl-4-carboxylic acid methyl ester 
• 1011478-18-4 3'-(4-chloro-2,5-dimethyl-benzenesulfonylamino)-3-methyl-biphenyl-4-carboxylic acid methyl ester 
• 1011479-54-1 3'-(4-chloro-2,5-dimethyl-benzenesulfonylamino)-3,5-dimethyl-biphenyl-4-carboxylic acid 
• 1021204-95-4 methyl 3-[1-(4-chloro-2,5-dimethyl-phenylsulfonyl)-piperidin-2-yl]-propionate 
• 1190971-03-9 3-(1-(4-chloro-2,5-dimethylphenylsulfonyl)piperidin-2-yl)propionic acid ethyl ester 
• 1155860-60-8 C₂₁H₂₃Cl₃N₂O₃S 
• 680972-87-6 3-[3-(R,S)-(4-chloro-2,5-dimethylbenzenesulfonyl)-4-oxo-2,5-benzodiazepin-3-yl]-N-[2-(pyridin-4-yl)ethyl]acetamide 
• 1372617-48-5 C₂₀H₃₁ClN₂O₇S 
• 1372617-67-8 C₁₈H₂₃ClN₂O₅S 

Relevant academic research and scientific papers

Substituted Disulfonamide Compounds

Substituted disulfonamide compounds corresponding to formula I: In which R1, R2, R3, R4a, R4b, R5a, R5b, R8, R9a, R9b, R10, R11, a, b, s, t and A have defined meanings, pharmaceutical compositions containing one or more such compounds, processes for preparing such compounds, and a method of using such compounds for the treatment or inhibition of pain and/or other conditions mediated by the bradykinin receptor 1 (BR1).

Phenylenediamine urotensin-II receptor antagonists and CCR-9 antagonists

The present invention relates to urotensin II receptor antagonists, CCR-9 antagonists, pharmaceutical compositions containing them and their use.