128366-02-9 Usage
Description
(3E)-3-[(ethylamino)(hydroxy)methylidene]quinoline-2,4(1H,3H)-dione, also known as ethylamino-quinoline-2,4-dione or ethylamino-6-hydroxy-2-methylene-3-quinuclidinone, is a quinoline derivative with potential pharmacological properties. It is a synthetic compound with a unique chemical structure that exhibits potential as a drug candidate for various therapeutic applications. (3E)-3-[(ethylamino)(hydroxy)methylidene]quinoline-2,4(1H,3H)-dione's chemical structure consists of a quinoline nucleus with an ethylamino group, a hydroxyl group, and a methylene group.
Uses
Used in Medicinal Chemistry:
(3E)-3-[(ethylamino)(hydroxy)methylidene]quinoline-2,4(1H,3H)-dione is used as a compound with potential pharmacological properties for the development of new drugs and therapies. Its unique chemical structure allows for exploration in various medicinal applications.
Used in Drug Development:
(3E)-3-[(ethylamino)(hydroxy)methylidene]quinoline-2,4(1H,3H)-dione is used as a potential drug candidate for the treatment of various diseases and conditions. Its unique chemical properties and potential pharmacological activities make it a valuable compound for further research and development in the pharmaceutical industry.
Used in Pharmaceutical Research:
(3E)-3-[(ethylamino)(hydroxy)methylidene]quinoline-2,4(1H,3H)-dione is used as a subject of study in pharmaceutical research to better understand its chemical properties, potential pharmacological activities, and possible applications in the development of new medications and therapies.
Check Digit Verification of cas no
The CAS Registry Mumber 128366-02-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,3,6 and 6 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 128366-02:
(8*1)+(7*2)+(6*8)+(5*3)+(4*6)+(3*6)+(2*0)+(1*2)=129
129 % 10 = 9
So 128366-02-9 is a valid CAS Registry Number.
128366-02-9Relevant articles and documents
4-Hydroxy-2-quinolones. 4. Selection of the Optimum Path for the Synthesis of N-R-Substituted 4-Hydroxy-2-quinolone-3-carboxylic Acid Amides
Ukrainets, I. V.,Bezuglyi, P. A.,Treskach, V. I.,Turov, A. V.
, p. 538 - 540 (2007/10/02)
A comparison of several methods of preparation of N-R-substituted 4-hydroxy-2-quinolone-3-carboxylic acid amides showed that intramolecular cyclization of 2-carbalkoxymalonanilic acid ethyl esters with simultaneous amidation is the most rational method.
