88511-13-1 Usage
Uses
Used in Energy Drinks and Supplements:
3-Aminothietane 1,1-dioxide is used as a performance enhancer for its potential to reduce muscle fatigue and improve athletic performance.
Used in Antioxidant Applications:
3-Aminothietane 1,1-dioxide is used as an antioxidant for its potential to protect the body from oxidative stress and support overall health.
Used in Cardiovascular Health:
3-Aminothietane 1,1-dioxide is used as a cardiovascular health supporter for its potential to help regulate fluid balance and support cardiovascular function.
Used in Digestive Health:
3-Aminothietane 1,1-dioxide is used as a digestive aid for its involvement in the formation of bile salts, which are necessary for the digestion and absorption of fats.
Check Digit Verification of cas no
The CAS Registry Mumber 88511-13-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,5,1 and 1 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 88511-13:
(7*8)+(6*8)+(5*5)+(4*1)+(3*1)+(2*1)+(1*3)=141
141 % 10 = 1
So 88511-13-1 is a valid CAS Registry Number.
88511-13-1Relevant academic research and scientific papers
Pathways in fission of strained rings
Diggle, Andrew W.,Griffiths, Gwerydd,Young, David J.,Stirling, Charles J. M.
, p. 317 - 321 (2007/10/02)
3-ring vs 4-ring reactivity ratios in the concerted cleavage of oxacycles are substantially smaller than for stepwise processes studied earlier but ratios are nevertheless much larger than strain energy differences could predict.In cleavage of hydroxycyclobutanes and of hydroxythietandioxides, activation parameters and substituent effects suggest a substantially greater degree of ring cleavage in the transition structure for the latter.For eliminative cleavage of a number of 3-substituted thietandioxides, there is no relationship between reactivity and the basicity of the 3-substituent; for "internal" carbon nucleophiles, however reactivities are in the order of the stabilising effects of substituents upon carbon-carbon double bonds.
