20600-63-9 Usage
Uses
Used in Pharmaceutical Industry:
ALLYLSULFANYL-ACETIC ACID is used as an active pharmaceutical ingredient for its potential anti-cancer properties. It is being researched for its ability to target and inhibit the growth of cancer cells, making it a promising candidate for the development of new cancer therapies.
Used in Chemical Synthesis:
ALLYLSULFANYL-ACETIC ACID is used as a building block and a key intermediate in the synthesis of various organic compounds. Its unique structure allows for the creation of a wide range of chemical entities, contributing to the advancement of chemical research and development.
Used in Anti-inflammatory Applications:
Due to its anti-inflammatory effects, ALLYLSULFANYL-ACETIC ACID is used in the development of treatments for inflammatory conditions. Its potential to modulate inflammatory responses can lead to the creation of new therapeutic agents for various diseases characterized by inflammation.
Used in Antioxidant Formulations:
ALLYLSULFANYL-ACETIC ACID is utilized in the formulation of antioxidant products due to its ability to neutralize free radicals and protect cells from oxidative damage. This makes it a valuable component in health supplements and skincare products aimed at promoting overall health and wellness.
Check Digit Verification of cas no
The CAS Registry Mumber 20600-63-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,6,0 and 0 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 20600-63:
(7*2)+(6*0)+(5*6)+(4*0)+(3*0)+(2*6)+(1*3)=59
59 % 10 = 9
So 20600-63-9 is a valid CAS Registry Number.
InChI:InChI=1/C5H8O2S/c1-2-3-8-4-5(6)7/h2H,1,3-4H2,(H,6,7)
20600-63-9Relevant academic research and scientific papers
Dicobalt hexacarbonyl complexes of alkynyl imines in a sequential Staudinger/Pauson-Khand process. A route to new fused tricyclic β-lactams
Olier, Clarisse,Azzi, Nadia,Gil, Gerard,Gastaldi, Stephane,Bertrand, Michele P.
supporting information; experimental part, p. 8469 - 8473 (2009/04/11)
(Chemical Equation Presented) Dicobalt hexacarbonyl complexes of alkynyl imines were allowed to react with ketenes via Staudinger reaction. Sequential [2 + 2] cycloaddition/Pauson-Khand reaction led to structurally new fused-tricyclic β-lactams and fused-
