6277-45-8 Usage
Description
1-[2-(4-methylphenyl)-2-oxoethyl]pyridinium is a chemical compound characterized by a pyridinium ring and a side chain that includes a 4-methylphenyl group and a 2-oxoethyl group. It is recognized for its potential as a corrosion inhibitor and its antimicrobial and antifungal properties. 1-[2-(4-methylphenyl)-2-oxoethyl]pyridinium is also of interest in pharmaceutical research and organic synthesis, serving as a key intermediate in the preparation of various compounds. Moreover, it has been studied for its potential therapeutic applications in treating diseases like cancer and Alzheimer's, attributed to its ability to modulate specific biological pathways. However, further research is necessary to fully comprehend its biological effects and potential applications.
Uses
Used in Organic Synthesis:
1-[2-(4-methylphenyl)-2-oxoethyl]pyridinium is used as a key intermediate in the synthesis of various organic compounds, contributing to the development of new chemical entities with diverse applications.
Used in Pharmaceutical Research:
In pharmaceutical research, 1-[2-(4-methylphenyl)-2-oxoethyl]pyridinium is utilized as a crucial component in the preparation of pharmaceuticals, potentially leading to the discovery of novel drugs with improved therapeutic effects.
Used as a Corrosion Inhibitor:
1-[2-(4-methylphenyl)-2-oxoethyl]pyridinium is employed as a corrosion inhibitor, helping to protect materials from degradation and extending their service life in various industrial applications.
Used for Antimicrobial and Anti-Fungal Applications:
1-[2-(4-methylphenyl)-2-oxoethyl]pyridinium is used for its antimicrobial and antifungal properties, making it a potential candidate for use in sanitizing products and treatments to combat microbial infections.
Used in Disease Treatment Research:
In the field of disease treatment research, 1-[2-(4-methylphenyl)-2-oxoethyl]pyridinium is studied for its potential use in treating various diseases, such as cancer and Alzheimer's, due to its ability to modulate certain biological pathways. Further research is required to explore its full therapeutic potential.
Check Digit Verification of cas no
The CAS Registry Mumber 6277-45-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,7 and 7 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6277-45:
(6*6)+(5*2)+(4*7)+(3*7)+(2*4)+(1*5)=108
108 % 10 = 8
So 6277-45-8 is a valid CAS Registry Number.
6277-45-8Relevant articles and documents
Cyclization of Active Methylene Isocyanides with α-Oxodithioesters Induced by Base: An Expedient Synthesis of 4-Methylthio/Ethoxycarbonyl-5-acylthiazoles
Anil, Seegehalli M.,Kiran, Kuppalli R.,Rajeev, Narasimhamurthy,Rangappa, Kanchugarakoppal S.,Sadashiva, Maralinganadoddi P.,Swaroop, Toreshettahally R.
, p. 1444 - 1450 (2020/04/27)
Cyclization of tosylmethyl isocyanide with α-oxodithioesters in the presence of KOH is reported for the synthesis of 4-methylthio-5-acylthiazoles. Similarly, ethyl isocyanoacetate underwent cyclization with α-oxodithioesters to form 4-ethoxycarbonyl-5-acy
Acid-Catalyzed Condensation of o-Phenylenediammines and o-Aminophenols with α-Oxodithioesters: A Divergent and Regio? selective Synthesis of 2-Methylthio-3-Aryl/Heteroarylquinoxalines and 2-Acylbenzoxazoles
Anil, Seegehally M,Kiran, Kuppalli R,Rangappa, Kanchugarakoppal S,Sadashiva, Maralinganadoddi P,Shruthi, Jeegundipattana B,Sukrutha, Kodipura P,Swaroop, Toreshettahally R
, p. 4205 - 4214 (2019/11/14)
o-Phenylenediammines and o-Aminophenols were reacted with α-oxodithioesters in a highly regioselective fashion to give 2-methylthio-3-Aryl/heteroarylquinoxalines and 2-Acylbenzoxazoles in 55-94percent and 45-86percent, respectively, in the presence of p-T
Coupling of azomethine ylides with nitrilium derivatives of closo-decaborate clusters: A synthetic and theoretical study
Mindich, Aleksey L.,Bokach, Nadezhda A.,Kuznetsov, Maxim L.,Haukka, Matti,Zhdanov, Andrey P.,Zhizhin, Konstantin Yu.,Miltsov, Serguei A.,Kuznetsov, Nikolay T.,Kukushkin, Vadim Yu.
, p. 1075 - 1086 (2013/03/13)
The azomethine ylides p-R3C5H4N+CHCOC 6H4R2-p (3a: R3=H, R2=H, X=Br; 3b: R3=H, R2=Me, X=I; 3c: R3=H, R2=OMe, X=I; 3d: R3=H, R2=F, X=I; 3e: R3=Me, R2=Me, X=Br) react with the nitrile functio
