69407-71-2 Usage
General Description
Ethyl 1-allyl-4-hydroxy-7-methyl-2-oxo-1,2-dihydro-1,8-naphthyridine-3-carboxylate is a chemical compound with a complex structure containing an ethyl ester group, allyl group, hydroxy group, and a naphthyridine ring. It is a synthetic compound that may have potential applications in pharmaceutical research and drug development. The compound's structure suggests that it may have biological activity due to the presence of the hydroxy and allyl groups, which are commonly found in many bioactive compounds. Further research and testing would be needed to determine its specific uses and potential benefits in various fields of science and medicine.
Check Digit Verification of cas no
The CAS Registry Mumber 69407-71-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,4,0 and 7 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 69407-71:
(7*6)+(6*9)+(5*4)+(4*0)+(3*7)+(2*7)+(1*1)=152
152 % 10 = 2
So 69407-71-2 is a valid CAS Registry Number.
69407-71-2Relevant articles and documents
2-Oxo-1,8-naphthyridine-3-carboxylic Acid Derivatives with Potent Gastric Antisecretory Properties
Santilli, Arthur A.,Scotese, Anthony C.,Bauer, Raymond F.,Bell, Stanley C.
, p. 2270 - 2277 (2007/10/02)
The syntheses of 2-oxo-1,8-naphthyridine-3-carboxylic acid derivatives having potent gastric antisecretory properties in the pyloric-ligated (Shay) rat model are described.Two of the more potent compounds tested that were selected for more detailed dose-r
4-Amino-3-carboxy or cyano-1,2-dihydro-2-oxo-1,8-naphthyridine derivatives
-
, (2008/06/13)
4-Amino-3-carboxy or cyano-1,2-dihydro-2-oxo-1,8-naphthyridine derivatives are anti-secretory agents for use in the treatment of peptic ulcer disease.
4-Hydroxy-pyrido[2,3-b]pyridine-2(1H)-one-3-carboxylic acids and esters
-
, (2008/06/13)
Anti-allergic 4-hydroxy-pyrido[2,3-b]pyridine-2(1H)-one-3-carboxylic acids and esters are prepared by reacting a 3,4-dihydro-1,3-dioxo-1H-pyrido[2,3-d][1,3]oxazine (a 3-azaisatoic anhydride) with an alkali metal salt of a malonic ester.
