61786-74-1 Usage
Description
(2E)-N-[2-(decylsulfanyl)-1-(hydroxymethyl)ethyl]-3-(6-methyl-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-5-yl)prop-2-enamide is a complex organic molecule with the molecular formula C23H35N3O4S. It is an amide derivative featuring a long carbon chain (decylsulfanyl) and a hydroxymethyl group. Additionally, it contains a pyrimidine ring with a methyl and two dioxo groups. (2E)-N-[2-(decylsulfanyl)-1-(hydroxymethyl)ethyl]-3-(6-methyl-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-5-yl)prop-2-enamide is an example of a complex organic molecule with multiple functional groups, which may have potential applications in medicinal, pharmaceutical, or chemical research. Its specific properties and potential uses would need to be investigated through further study and analysis.
Uses
Used in Medicinal Applications:
(2E)-N-[2-(decylsulfanyl)-1-(hydroxymethyl)ethyl]-3-(6-methyl-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-5-yl)prop-2-enamide is used as a potential pharmaceutical agent for its unique structure and functional groups. (2E)-N-[2-(decylsulfanyl)-1-(hydroxymethyl)ethyl]-3-(6-methyl-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-5-yl)prop-2-enamide's specific interactions with biological targets and its potential therapeutic effects need to be explored through further research.
Used in Chemical Research:
In the field of chemical research, (2E)-N-[2-(decylsulfanyl)-1-(hydroxymethyl)ethyl]-3-(6-methyl-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-5-yl)prop-2-enamide serves as a subject for studying the synthesis, reactivity, and properties of complex organic molecules. Its structure can provide insights into the development of new synthetic pathways and the exploration of novel chemical reactions.
Used in Pharmaceutical Development:
(2E)-N-[2-(decylsulfanyl)-1-(hydroxymethyl)ethyl]-3-(6-methyl-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-5-yl)prop-2-enamide is used as a candidate for drug development due to its unique molecular structure and functional groups. (2E)-N-[2-(decylsulfanyl)-1-(hydroxymethyl)ethyl]-3-(6-methyl-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-5-yl)prop-2-enamide may exhibit specific biological activities that could be harnessed for the treatment of various diseases or conditions, pending further investigation and validation.
Check Digit Verification of cas no
The CAS Registry Mumber 61786-74-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,7,8 and 6 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 61786-74:
(7*6)+(6*1)+(5*7)+(4*8)+(3*6)+(2*7)+(1*4)=151
151 % 10 = 1
So 61786-74-1 is a valid CAS Registry Number.
61786-74-1Relevant articles and documents
Pyrimidinylpropenamides as antitumor agents. Analogues of the antibiotic sparsomycin
Lin,Dubois
, p. 337 - 341 (2007/10/06)
A series of pyrimidinylpropenamides 9 and their oxidation products 10 was prepared, as analogues of sparsomycin (1), for antitumor evaluation. Syntheses involved condensation of the appropriate amino alcohol 5 with acid 8. The resulting sulfides 9 were then oxidized with NaIO4 or H2O2 to sulfoxides 10. Activity was studied in lymphocytic leukemia P-388 and KB cell culture. With the exception of the n-decyl analogue, all of the deoxygenated compounds 9 were inactive regardless of the sterochemical form. In the sulfoxide series 10, those compounds prepared with an L configuration at the asymmetric carbon were also inactive. The completely racemic sulfoxides, on the other hand, displayed substantial antitumor activity (ILS=37-61% in P-388; ED50=1.2-2.4μg/ml in KB) suggesting that both the presence of a sulfoxide moiety and a D configuration at the chiral carbon atom were structural requirements for a positive antitumor response. There appeared to be a large tolerance for the group substituted at the sulfoxide moiety, however.
