164464-60-2 Usage
Uses
Used in Pharmaceutical Industry:
Ethyl 2-chloropyridine-3-carboxylate is used as an intermediate for the production of pyridine-based compounds, which are integral in the development of various drugs. Its presence in the synthesis process is vital for creating a range of pharmaceutical products.
Used in Agrochemical Industry:
Similarly, in the agrochemical sector, Ethyl 2-chloropyridine-3-carboxylate is employed as a starting material in the synthesis of compounds used in agricultural chemicals, contributing to the development of effective crop protection agents and other related products.
Used in Organic Synthesis:
Ethyl 2-chloropyridine-3-carboxylate is also utilized as a solvent or reagent in chemical reactions, highlighting its versatility in organic synthesis. Its role in these processes is essential for the creation of a wide array of chemical products.
Check Digit Verification of cas no
The CAS Registry Mumber 164464-60-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,4,4,6 and 4 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 164464-60:
(8*1)+(7*6)+(6*4)+(5*4)+(4*6)+(3*4)+(2*6)+(1*0)=142
142 % 10 = 2
So 164464-60-2 is a valid CAS Registry Number.
164464-60-2Relevant academic research and scientific papers
Antiviral thiazoles
-
, (2008/06/13)
Compounds of formula (I) are active antiviral compounds useful in the treatment of viral infections in mammals. The compounds of the invention are readily prepared by reaction of a suitable 2-thiothiazole derivative with an appropriate Het-(CH2)n -halide.
The synthesis of thienopyridines from ortho-halogenated pyridine derivatives; Part 2
Bremner,Dunn,Wilson,Sturrock,Wishart
, p. 949 - 952 (2007/10/03)
Synthetic routes to the ortho-halogenated pyridine derivatives, ethyl 2- and 4-chloro-3-pyridylacetate, ethyl 3-bromo-4-pyridylacetate and ethyl 3-bromo-2-pyridylacetate, which have methylene groups activated by the ester functionality are reported. Reaction of these pyridines with carbon disulfide in the presence of sodium hydride, followed by quenching with iodomethane, results in the formation of the corresponding thienopyridines in moderate yields.
