175137-71-0 Usage
Uses
Used in Organic Synthesis:
2-([2-[(4-Chlorophenyl)sulfonyl]ethyl]thio)acetic acid is utilized as a building block in organic synthesis, providing a foundation for the creation of a diverse array of organic compounds. Its presence of sulfonyl and thioether groups enhances its reactivity, making it a valuable component in the synthesis of complex molecules.
Used in Pharmaceutical Development:
In the pharmaceutical industry, 2-([2-[(4-Chlorophenyl)sulfonyl]ethyl]thio)acetic acid serves as a starting material for the preparation of various pharmaceuticals. Its unique structure and functional groups allow for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Production:
2-([2-[(4-Chlorophenyl)sulfonyl]ethyl]thio)acetic acid is also employed in the agrochemical sector, where it is used as a precursor for the synthesis of various agrochemicals. Its properties make it suitable for the development of compounds that can be used in crop protection and other agricultural applications.
Used in Material and Polymer Development:
Due to its unique structure and functional groups, 2-([2-[(4-Chlorophenyl)sulfonyl]ethyl]thio)acetic acid has potential applications in the development of new materials and polymers. Its versatility and reactivity contribute to the creation of innovative materials with specific properties tailored for various industrial uses.
Check Digit Verification of cas no
The CAS Registry Mumber 175137-71-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,5,1,3 and 7 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 175137-71:
(8*1)+(7*7)+(6*5)+(5*1)+(4*3)+(3*7)+(2*7)+(1*1)=140
140 % 10 = 0
So 175137-71-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H11ClO4S2/c11-8-1-3-9(4-2-8)17(14,15)6-5-16-7-10(12)13/h1-4H,5-7H2,(H,12,13)
175137-71-0Relevant academic research and scientific papers
Synthesis of a new class of arylsulfonylethylsulfonylmethyloxazolines and thiazolines
Padmavathi, Venkatapuram,Venkatesh, Bhumireddy Chinnachennaiahgari,Premakumari, Chokkappagari,Padmaja, Adivireddy
, p. 646 - 651 (2012/09/07)
A new class of arylsulfonylethylsulfonylmethyl oxazolines and thiazolines were prepared using multistep, one-pot methodologies exploiting lanthanide alkoxides and under microwave irradiation. The microwave method provides an excellent approach in a single step with high yields.
