75606-68-7 Usage
Molecular Weight
211.36 g/mol
Structure
A seven-carbon chain with a double bond at the third and sixth positions, a thiazolidine ring, and a methyl group attached to the ring.
Group
Thiazolidine derivatives
Biological Activities
Anti-inflammatory, antioxidant, and antimicrobial properties
Potential Applications
Pharmaceuticals or other industries due to unique structure and biological activities
Extensive Studies
The specific properties and uses of this compound have not been extensively studied.
Check Digit Verification of cas no
The CAS Registry Mumber 75606-68-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,6,0 and 6 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 75606-68:
(7*7)+(6*5)+(5*6)+(4*0)+(3*6)+(2*6)+(1*8)=147
147 % 10 = 7
So 75606-68-7 is a valid CAS Registry Number.
InChI:InChI=1/C11H19NS/c1-3-4-5-6-7-8-11(2)12-9-10-13-11/h3,5-6,12H,1,4,7-10H2,2H3/b6-5+
75606-68-7Relevant articles and documents
Synthesis and radiopharmacological study of unsaturated derivatives of cysteamine
Mesnard,Miginiac,Fatome,et al.
, p. 247 - 252 (2007/10/02)
Synthesis of many unsaturated compounds derivated from cysteamine has been carried out in the three series : β-aminothioethers, β-aminothiols and thiazolidines. These products are more or less toxic, compared to corresponding saturated derivates. They generally have a higher radioprotective activity. The three most effective have a dose reduction factor equivalent to that of cysteamine, two of them having a lower toxicity.