3545-51-5 Usage
Uses
Used in Pharmaceutical Research:
1-(3-phenylpropyl)pyrimidine-2,4(1H,3H)-dione is used as a research compound for its potential therapeutic applications in the pharmaceutical industry. Its unique structure and properties make it a candidate for further exploration in drug development and medicinal chemistry.
Used in Drug Development:
In the field of drug development, 1-(3-phenylpropyl)pyrimidine-2,4(1H,3H)-dione is utilized as a promising candidate for the creation of novel therapeutic agents. Its specific biological and pharmacological properties are being investigated to understand its potential in treating various medical conditions.
Used in Medicinal Chemistry:
1-(3-phenylpropyl)pyrimidine-2,4(1H,3H)-dione serves as a valuable compound in medicinal chemistry, where it is employed for the design and synthesis of new drugs. Its unique structure allows researchers to explore its interactions with biological targets, potentially leading to the development of innovative therapeutic solutions.
Check Digit Verification of cas no
The CAS Registry Mumber 3545-51-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,4 and 5 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3545-51:
(6*3)+(5*5)+(4*4)+(3*5)+(2*5)+(1*1)=85
85 % 10 = 5
So 3545-51-5 is a valid CAS Registry Number.
3545-51-5Relevant academic research and scientific papers
SMALL MOLECULES AGAINST CEREBLON TO ENHANCE EFFECTOR T CELL FUNCTION
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Page/Page column 172; 181-182, (2017/10/11)
Disclosed are small molecules against cereblon to enhance effector T cell function. Methodos of making thes molecules and methods of using them to treat various disease states are also disclosed.
One-pot protocol for N-alkylation of purine, pyrimidine and azole derivatives via alcohols using Ph3P/I2: simple route for carboacyclic nucleoside synthesis
Soltani Rad, Mohammad Navid,Soleimani, Faezeh
supporting information, p. 4947 - 4953 (2016/07/19)
A simple and efficient synthetic protocol for the one-pot N-alkylation of nucleobases and their related N-heterocycles via alcohols utilizing the combination of PPh3and I2is reported. In this protocol purine, pyrimidine and azole derivatives underwent the N-alkylation reaction with diverse primary alcohols using Ph3P/I2in the presence of Et3N-K2CO3in anhydrous DMF to give the N-alkyl adducts (carboacyclic nucleosides) in good yields (up to 90%). The influence of some parameters in this reaction including type of solvent, base, reagents and temperature was discussed. In addition, this protocol has proved the favorable selectivity towards primary hydroxyl versus secondary hydroxyl group in diols.
