117671-03-1 Usage
Uses
Used in Organic Synthesis:
Methyl 2-fluoro-6-methoxynicotinate is utilized as a key intermediate in the synthesis of various organic compounds. Its unique structure allows for the creation of a wide range of chemical entities, making it a versatile component in the development of novel organic molecules.
Used in Pharmaceutical Research:
In the pharmaceutical industry, methyl 2-fluoro-6-methoxynicotinate serves as a crucial building block for the development of new drugs. Its incorporation into drug candidates can potentially enhance their efficacy, selectivity, and pharmacokinetic properties, leading to improved therapeutic outcomes.
Used in Agrochemical Development:
Methyl 2-fluoro-6-methoxynicotinate is also employed in the agrochemical sector for the development of new pesticides and other crop protection agents. Its unique chemical properties can contribute to the creation of more effective and environmentally friendly agrochemicals.
Used in Medicinal Chemistry for Biological Activity Studies:
Due to its potential biological activities, methyl 2-fluoro-6-methoxynicotinate is an interesting target for investigation in medicinal chemistry. Researchers explore its interactions with biological targets to understand its therapeutic potential and to develop new drugs with novel mechanisms of action.
Check Digit Verification of cas no
The CAS Registry Mumber 117671-03-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,6,7 and 1 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 117671-03:
(8*1)+(7*1)+(6*7)+(5*6)+(4*7)+(3*1)+(2*0)+(1*3)=121
121 % 10 = 1
So 117671-03-1 is a valid CAS Registry Number.
117671-03-1Relevant academic research and scientific papers
Nickel-Catalyzed Oxidative Decarboxylative Annulation for the Synthesis of Heterocycle-Containing Phenanthridinones
Honeycutt, Aaron P.,Hoover, Jessica M.
, p. 7216 - 7219 (2018/11/23)
A nickel-catalyzed oxidative decarboxylative annulation reaction of simple benzamides and (hetero)aromatic carboxylates has been developed. This reaction provides access to a large array of phenanthridinones and their heterocyclic analogues, highlighting the utility and versatility of oxidative decarboxylative coupling strategies for C-C bond formation.
An efficient synthesis of 5-bromo-2-methoxy-6-methylaminopyridine-3-carboxylic acid
Hirokawa,Horikawa,Kato
, p. 1847 - 1853 (2007/10/03)
An efficient synthesis of 5-bromo-2-methoxy-6-methylaminopyridine-3-carboxylic acid (1), a carboxylic acid moiety of a potent dopamine D2 and D3 and serotonin-3 (5-HT3) receptors antagonist, (R)-5-bromo-N-(1-ethyl-4-methyl
