70648-87-2 Usage
Uses
Used in Pharmaceutical Industry:
2-[(2-ANILINO-2-OXOETHYL)SULFANYL]ACETIC ACID is used as a potential therapeutic agent for its antioxidant properties, which can help in combating oxidative stress-related conditions. Its free radical scavenging ability makes it a candidate for treating diseases associated with oxidative damage.
Used in Anti-inflammatory Applications:
In the medical field, 2-[(2-ANILINO-2-OXOETHYL)SULFANYL]ACETIC ACID is utilized as an anti-inflammatory agent, potentially mitigating inflammation through its effects on inflammatory pathways and reducing associated symptoms.
Used in Analgesic Applications:
2-[(2-ANILINO-2-OXOETHYL)SULFANYL]ACETIC ACID is also considered for its analgesic properties, suggesting its use in pain management, particularly where oxidative stress and inflammation are contributing factors.
Used in Antioxidant Formulations:
As a component in antioxidant formulations, 2-[(2-ANILINO-2-OXOETHYL)SULFANYL]ACETIC ACID can be used to protect cells from damage caused by reactive oxygen species, which has implications for a variety of health and skincare products.
Used in Research and Development:
In the scientific community, 2-[(2-ANILINO-2-OXOETHYL)SULFANYL]ACETIC ACID serves as a subject of research for exploring its potential mechanisms of action and further understanding its role in biological systems, which could lead to the development of new therapeutic strategies.
Check Digit Verification of cas no
The CAS Registry Mumber 70648-87-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,6,4 and 8 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 70648-87:
(7*7)+(6*0)+(5*6)+(4*4)+(3*8)+(2*8)+(1*7)=142
142 % 10 = 2
So 70648-87-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H11NO3S/c12-9(6-15-7-10(13)14)11-8-4-2-1-3-5-8/h1-5H,6-7H2,(H,11,12)(H,13,14)
70648-87-2Relevant academic research and scientific papers
Synthesis and dynamic stereochemistry of 4-aryl-thiomorpholine-3,5-dione derivatives
Szawka?o, Joanna,Maurin, Jan K.,Pluciński, Franciszek,Czarnocki, Zbigniew
, p. 383 - 390 (2014/12/10)
A series of new N-aryl-substituted thiomorpholine-3,5-diones were synthesized. Crystal structures of seven compounds were established on the basis of X-ray crystallography. Stable at room temperature diastereomers were detected for (2-phenyl)-substituted derivatives using 1H NMR. The dynamic stereochemistry of compound 36 was studied with variable-temperature 1H NMR and the mechanism of diastereomers interconversion was proposed on the basis of quantum chemical calculations.
Synthesis and pyrolysis of tetrahydro-1,4-oxazine-3,5-diones and tetrahydro-1,4-thiazine-3,5-diones
Aitken,Farrell,Kirton
, p. 1526 - 1531 (2007/10/03)
The preparation and characterization of six 4-substituted tetrahydro-l,4-oxazine-3,5-diones and five 4-substituted tetrahydro-l,4-thiazine-3,5-diones is described. Upon flash vacuum pyrolysis at 700°C these give N-substituted acetamides and nitriles, and a mechanism for formation of these products is proposed.
