69536-71-6 Usage
Uses
Used in Biochemical and Pharmaceutical Research:
2-(Acetylsulfanyl)ethanesulphonic is used as a buffer solution for maintaining stable pH conditions in biochemical and pharmaceutical research, facilitating various experimental procedures and analyses.
Used in Pharmaceutical Drug Production:
2-(Acetylsulfanyl)ethanesulphonic is used as a key component in the production of various pharmaceutical drugs, contributing to their efficacy and stability.
Used in Chemical Synthesis:
2-(Acetylsulfanyl)ethanesulphonic is used as a reagent in the synthesis of various organic compounds, enabling the creation of new chemical entities with potential applications in different fields.
Used in Industrial Processes:
2-(Acetylsulfanyl)ethanesulphonic is used as a stabilizing agent in various industrial processes, ensuring the consistency and quality of the final products.
Used in Polymer Production:
2-(Acetylsulfanyl)ethanesulphonic is used in the production of certain polymers, contributing to their properties and performance in various applications.
Used as a Catalyst in Chemical Reactions:
2-(Acetylsulfanyl)ethanesulphonic is used as a catalyst to accelerate chemical reactions, improving the efficiency and yield of the processes.
Check Digit Verification of cas no
The CAS Registry Mumber 69536-71-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,5,3 and 6 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 69536-71:
(7*6)+(6*9)+(5*5)+(4*3)+(3*6)+(2*7)+(1*1)=166
166 % 10 = 6
So 69536-71-6 is a valid CAS Registry Number.
69536-71-6Relevant academic research and scientific papers
Sanden, Sebastian A.,Yi, Ruiqin,Hara, Masahiko,McGlynn, Shawn E.
, p. 11989 - 11992 (2020)
Thioesters are important intermediates in both synthetic organic and biosynthetic reaction pathways. Here we show that thioesters can be synthesized in an aqueous reaction between thioacetate and thiols. The reaction can be coupled to a second reaction between sulfide and either ferrous or ferric iron, which drives the reaction forward. We furthermore demonstrate that sulfide released during thioester formation can be used in the synthesis of peptide bound [Fe-S] clusters, which like thioesters, are ancient components of metabolism. Together our results reveal a primordial linkage between high-energy ester formation and redox chemistry.
