78893-39-7 Usage
Uses
Used in Pharmaceutical Industry:
(4E)-4-[(dimethylamino)methylidene]-6,7-dimethoxy-1,4-dihydroisoquinolin-3(2H)-one serves as a synthetic intermediate for the development of pharmaceuticals. Its complex structure and functional groups contribute to the creation of new medicinal compounds that can address various health conditions.
Used in Organic Synthesis:
In the field of organic synthesis, (4E)-4-[(dimethylamino)methylidene]-6,7-dimethoxy-1,4-dihydroisoquinolin-3(2H)-one is employed as a key component in the synthesis of a variety of organic molecules. Its unique structure allows for the formation of diverse chemical entities with potential applications in different industries.
Used in Research and Development:
(4E)-4-[(dimethylamino)methylidene]-6,7-dimethoxy-1,4-dihydroisoquinolin-3(2H)-one is utilized in research and development settings to explore its potential biological activities. Scientists are interested in investigating its properties to uncover new therapeutic applications and to enhance the understanding of its interactions with biological systems.
Check Digit Verification of cas no
The CAS Registry Mumber 78893-39-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,8,9 and 3 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 78893-39:
(7*7)+(6*8)+(5*8)+(4*9)+(3*3)+(2*3)+(1*9)=197
197 % 10 = 7
So 78893-39-7 is a valid CAS Registry Number.
78893-39-7Relevant academic research and scientific papers
Acetals of Lactams and Acid Amides. 34. Synthesis and Properties of Enamines of the Isoquinoline Series
Knyazeva, V. F.,Granik, V. G.,Glushkov, R. G.,Solov'eva, N. P.,Anisimova, O. S.
, p. 370 - 374 (2007/10/02)
The reactions of 1,2,3,4-tetrahydro-3-isoquinolone derivatives with dimethylformamide acetal and the hydrolysis and transamination of the resulting enamino amides - 1,2,3,4-tetrahydro-4-dimethylaminomethylene-3-isoquinolone derivatives - were studied.It is shown that 1,2,3,4-tetrahydro-1-phenyl-6,7-dimethoxy-3-isoquinolone can be converted to the corresponding lactim ether.The reactions of the latter with dimethylformamide acetal and hydrazine and the dehydrogenation of this lactim ether in the presence of sodium ethoxide were studied.
