106960-78-5 Usage
Description
ETHYL 5-OXO-5,6,7,8-TETRAHYDROQUINOLINE-3-CARBOXYLATE is a chemical compound with the formula C13H15NO3, belonging to the class of organic compounds known as tetrahydroquinolines. It features a quinoline moiety, which is a bicyclic aromatic compound consisting of a pyridine ring fused to a benzene ring, and is substituted by one alkyl group, an oxo group, and one carboxylate group. ETHYL 5-OXO-5,6,7,8-TETRAHYDROQUINOLINE-3-CARBOXYLATE's physical properties, such as solubility, stability, and hazard levels, can vary depending on its usage, preparation method, or storage conditions.
Uses
ETHYL 5-OXO-5,6,7,8-TETRAHYDROQUINOLINE-3-CARBOXYLATE does not have extensive common usage and is primarily utilized in scientific and industrial research or processes. Its specific applications may include:
Used in Scientific Research:
ETHYL 5-OXO-5,6,7,8-TETRAHYDROQUINOLINE-3-CARBOXYLATE is used as a research compound for studying its chemical properties, potential reactions, and possible applications in various fields.
Used in Industrial Processes:
In the chemical industry, ETHYL 5-OXO-5,6,7,8-TETRAHYDROQUINOLINE-3-CARBOXYLATE may be used as an intermediate in the synthesis of other compounds or as a component in specific formulations.
Check Digit Verification of cas no
The CAS Registry Mumber 106960-78-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,9,6 and 0 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 106960-78:
(8*1)+(7*0)+(6*6)+(5*9)+(4*6)+(3*0)+(2*7)+(1*8)=135
135 % 10 = 5
So 106960-78-5 is a valid CAS Registry Number.
106960-78-5Relevant articles and documents
A Facile Synthesis of Polyfunctionally Substituted Pyridines from Ethoxycarbonylmalonaldehyde
Torii, Sigeru,Inokuchi, Tsutomu,Kubota, Minoru
, p. 400 - 402 (2007/10/02)
A facile access to 2,3-disubstituted-5-ethoxycarbonylpyridines (50-66percent yields), derivatives of biologically and medicinally important nicotinic acid, is explored.The method involves the reaction of ethoxycarbonylmalonaldehyde with tosyl chloride and then with β-amino-α,β-unsaturated esters, ketones, or nitriles in the presence of pyridine.
