21203-55-4 Usage
Uses
Used in Pharmaceutical and Agrochemical Synthesis:
2,4,6-Trimethyl-3-nitropyridine is used as a key intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its unique chemical structure allows for the development of new compounds with potential therapeutic and pesticidal properties.
Used in Organic Chemistry Research:
In research laboratories, 2,4,6-trimethyl-3-nitropyridine is employed as a reagent for various organic chemistry applications. Its versatility in chemical reactions contributes to the advancement of scientific knowledge and the discovery of novel chemical compounds.
Used in Industrial Settings:
2,4,6-Trimethyl-3-nitropyridine is utilized in industrial settings for the large-scale production of pharmaceuticals and agrochemicals. Its stability and solubility properties make it suitable for use in manufacturing processes.
It is crucial to handle 2,4,6-trimethyl-3-nitropyridine with care and adhere to proper safety procedures to minimize health risks associated with exposure to 2.4.6-TRIMETHYL-3-NITROPYRIDINE.
Check Digit Verification of cas no
The CAS Registry Mumber 21203-55-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,2,0 and 3 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 21203-55:
(7*2)+(6*1)+(5*2)+(4*0)+(3*3)+(2*5)+(1*5)=54
54 % 10 = 4
So 21203-55-4 is a valid CAS Registry Number.
InChI:InChI=1/C8H10N2O2/c1-5-4-6(2)9-7(3)8(5)10(11)12/h4H,1-3H3
21203-55-4Relevant academic research and scientific papers
As potassium channel regulator compound
-
Paragraph 0163; 0164; 0165, (2017/07/14)
The invention relates to a compound taken as a potassium channel regulator. The compound taken as the potassium channel regulator is a compound shown in a formula (I) or pharmaceutically acceptable salt thereof, and the compound or pharmaceutically accept
Purin-8-ones as corticotropin-releasing hormone (CRH-R1) receptor antagonists
Beck, James P.,Arvanitis, Argyrios G.,Curry, Matt A.,Rescinito, Joseph T.,Fitzgerald, Larry W.,Gilligan, Paul J.,Zaczek, Robert,Trainor, George L.
, p. 967 - 972 (2007/10/03)
A series of purin-8-ones was prepared and discovered to have excellent binding affinity to the CRH-R1 receptor. Structure-activity studies focused on amine side-chain optimization, urea substitution and pyridyl isostere incorporation. Thus, the highly potent purin-8-ones show promise as a new class of potential anxiolytics and/or antidepressants.
Synthesis of indoles from pyridinium salts. 7. Sterically hindered alkyl-3-nitropyridinium salts in the synthesis of indoles
Yurovskaya,Afanas'ev,Druzina,Bundel'
, p. 667 - 672 (2007/10/02)
The introduction of bulky alkyl substituents (iso-Pr,tert-Bu) into any positions of the starting 3-nitropyridinium salt only increases the reaction time and decreases the yields of the corresponding alkylindoles somewhat.
