5810-64-0 Usage
Uses
Used in Pharmaceutical Industry:
(5Z)-1-(3-chlorophenyl)-5-[(2E)-3-(2-nitrophenyl)prop-2-en-1-ylidene]-2-thioxodihydropyrimidine-4,6(1H,5H)-dione is used as a potential pharmaceutical compound for its unique structure and the possibility of targeting specific biological pathways. The presence of the 3-chlorophenyl and 2-nitrophenyl groups, along with the thioxo and prop-2-en-1-ylidene moieties, may allow for interactions with various biological targets, making it a candidate for drug development.
Used in Chemical Research:
In the field of chemical research, (5Z)-1-(3-chlorophenyl)-5-[(2E)-3-(2-nitrophenyl)prop-2-en-1-ylidene]-2-thioxodihydropyrimidine-4,6(1H,5H)-dione serves as a subject for studying the synthesis, reactivity, and potential applications of complex organic molecules. Its unique structure may provide insights into new reaction mechanisms and the development of novel synthetic methods.
Used in Material Science:
(5Z)-1-(3-chlorophenyl)-5-[(2E)-3-(2-nitrophenyl)prop-2-en-1-ylidene]-2-thioxodihydropyrimidine-4,6(1H,5H)-dione may also find applications in material science, particularly in the development of new materials with specific properties. (5Z)-1-(3-chlorophenyl)-5-[(2E)-3-(2-nitrophenyl)prop-2-en-1-ylidene]-2-thioxodihydropyrimidine-4,6(1H,5H)-dione's structure could potentially be utilized to create materials with unique optical, electronic, or mechanical characteristics.
Check Digit Verification of cas no
The CAS Registry Mumber 5810-64-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,1 and 0 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5810-64:
(6*5)+(5*8)+(4*1)+(3*0)+(2*6)+(1*4)=90
90 % 10 = 0
So 5810-64-0 is a valid CAS Registry Number.
5810-64-0Relevant academic research and scientific papers
Convenient synthesis of 2-substituted 5,7-dihydro-6H-pyrrolo[2,3-d]pyrimidin-6-ones
Kókai, Eszter,Nagy, József,Tóth, Tünde,Kupai, József,Huszthy, Péter,Simig, Gyula,Volk, Balázs
, p. 767 - 773 (2016/03/23)
A new synthetic route was elaborated at our laboratory providing a convenient access to 5,7-dihydro-6H-pyrrolo[2,3-d]pyrimidin-6-ones (diazaoxindoles), a compound family of biological relevance. Treatment of the easily available ethyl 2-(4-chloropyrimidin-5-yl)acetate derivatives with ammonia afforded the corresponding 2-(4-aminopyrimidin-5-yl)acetamides, which were finally cyclized to the target compounds.
