53389-00-7 Usage
General Description
Ethyl 6-hydroxypyridine-2-carboxylate is a chemical compound with the molecular formula C9H9NO3. It is a derivative of pyridine and is commonly used in the synthesis of pharmaceuticals and agrochemicals. ETHYL 6-HYDROXYPYRIDINE-2-CARBOXYLATE has been reported to have antioxidant and anti-inflammatory properties, making it potentially valuable for medical and cosmetic applications. It is a clear, colorless liquid with a characteristic odor and is typically stored and handled in a controlled laboratory setting due to its potential health hazards. Overall, ethyl 6-hydroxypyridine-2-carboxylate has a variety of industrial uses and may have potential therapeutic benefits.
Check Digit Verification of cas no
The CAS Registry Mumber 53389-00-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,3,8 and 9 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 53389-00:
(7*5)+(6*3)+(5*3)+(4*8)+(3*9)+(2*0)+(1*0)=127
127 % 10 = 7
So 53389-00-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H9NO3/c1-2-12-8(11)6-4-3-5-7(10)9-6/h3-5H,2H2,1H3,(H,9,10)
53389-00-7Relevant articles and documents
TRIAZOLOPYRIMIDINE DERIVATIVES FOR USE AS GHRELIN O-ACYL TRANSFERASE (GOAT) INHIBITORS
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Page/Page column 62, (2019/08/26)
The present invention relates to compounds of general formula I, wherein the groups R1 and R2 are defined as in claim 1, which have valuable pharmacological properties, in particular bind to ghrelin O-acyl transferase (GOAT) and modulate its activity. The compounds are suitable for treatment and prevention of diseases which can be influenced by this receptor, such as metabolic diseases, in particular obesity.
An annulation method for the synthesis of alkyl-substituted 6-carbomethoxy-2-pyridones
Zhang, Yu,Loertscher, Brad M.,Castle, Steven L.
experimental part, p. 6584 - 6590 (2011/02/25)
A protocol for the synthesis of 5-alkyl and 3,5-dialkyl-6-carbomethoxy-2-pyridones was devised. Key steps include a Mannich reaction, acylation of a tosylamine, and a PPh3/TiCl4-promoted intramolecular Reformatsky-type reaction with
