58742-72-6 Usage
Uses
Used in Pharmaceutical Industry:
N-Methyl-N-(Methylsulfonyl)glycine Ethyl Ester is used as a nonsteroidal anti-inflammatory drug for its ability to reduce pain and inflammation. It is particularly effective due to its capacity to inhibit the production of prostaglandins, which are integral to the body's inflammatory response and pain sensation.
Used in Pain Management:
In the field of pain management, N-Methyl-N-(Methylsulfonyl)glycine Ethyl Ester serves as an analgesic agent, helping to alleviate various types of pain by interfering with the prostaglandin synthesis pathway, thus providing relief to patients suffering from different painful conditions.
Used in Inflammation Treatment:
For the treatment of inflammation, N-Methyl-N-(Methylsulfonyl)glycine Ethyl Ester acts as an anti-inflammatory agent, reducing the signs and symptoms of inflammation by targeting the biochemical processes that lead to tissue swelling and discomfort.
Further research is necessary to fully understand the breadth of applications and the mechanisms by which N-Methyl-N-(Methylsulfonyl)glycine Ethyl Ester exerts its therapeutic effects, potentially expanding its use in medicine.
Check Digit Verification of cas no
The CAS Registry Mumber 58742-72-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,7,4 and 2 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 58742-72:
(7*5)+(6*8)+(5*7)+(4*4)+(3*2)+(2*7)+(1*2)=156
156 % 10 = 6
So 58742-72-6 is a valid CAS Registry Number.
58742-72-6Relevant academic research and scientific papers
N, N -Bis-(dimethylfluorosilylmethyl)amides of N -organosulfonylproline and sarcosine: Synthesis, structure, stereodynamic behaviour and in silico studies
Nikolin, Alexey A.,Kramarova, Eugenia P.,Shipov, Alexander G.,Baukov, Yuri I.,Negrebetsky, Vadim V.,Arkhipov, Dmitry E.,Korlyukov, Alexander A.,Lagunin, Alexey A.,Bylikin, Sergey Yu.,Bassindale, Alan R.,Taylor, Peter G.
, p. 75315 - 75327 (2016/08/24)
(O→Si)-Chelate difluorides R3R2NCH(R1)C(O)N(CH2SiMe2F)2 (9a-c, R1R2 = (CH2)3, R3 = Ms (a), Ts (b); R1 = H, R2 = Me, R3 = Ms (c)), containing one penta- and one tetracoordinate silicon atoms were synthesized by silylmethylation of amides R3R2NCH(R1)C(O)NH2, subsequent hydrolysis of unstable intermediates R3R2NCH(R1)C(O)N(CH2SiMe2Cl)2 (7a-c) into 4-acyl-2,6-disilamorpholines R3R2NCH(R1)C(O)N(CH2SiMe2O)2 (8a-c) and the reaction of the latter compounds with BF3·Et2O. The structures of disilamorpholines 8a,c and difluoride 9a were confirmed by an X-ray diffraction study. According to the IR and NMR data, the O→Si coordination in solutions of these compounds was weaker than that in the solid state due to effective solvation of the Si-F bond. A permutational isomerisation involving an exchange of equatorial Me groups at the pentacoordinate Si atom in complexes 9a-c was detected, and its activational parameters were determined by 1H DNMR. In silico estimation of possible pharmacological effects and acute rat toxicity by PASS Online and GUSAR Online services showed a potential for their further pharmacological study.
