63502-76-1 Usage
Uses
Used in Pharmaceutical Research and Drug Development:
2,4(1H,3H)-Pyrimidinedione, 1-cyclohexyl-5-fluorois utilized as a key compound in pharmaceutical research and drug development due to its potential biological activities. Its unique structure allows it to interact with specific proteins in cancer cells, making it a promising candidate for the development of anticancer drugs.
Used in Anticancer Applications:
In the field of oncology, 2,4(1H,3H)-Pyrimidinedione, 1-cyclohexyl-5-fluorois employed as a potential anticancer agent. It targets specific proteins within cancer cells, which can inhibit tumor growth and progression. Its potential as an anticancer drug is currently under investigation, with the aim of developing more effective treatments for various types of cancer.
Used in Anti-inflammatory and Analgesic Applications:
2,4(1H,3H)-Pyrimidinedione, 1-cyclohexyl-5-fluorohas also shown potential as an anti-inflammatory and analgesic agent. Its ability to modulate the body's inflammatory response and alleviate pain makes it a valuable compound in the study and treatment of various diseases and disorders, particularly those involving inflammation and pain management.
Used in Chemical Synthesis:
In the chemical industry, 2,4(1H,3H)-Pyrimidinedione, 1-cyclohexyl-5-fluorocan be used as a starting material or intermediate in the synthesis of other complex molecules. Its unique structure and reactivity make it a versatile building block for the creation of new compounds with potential applications in various fields, including pharmaceuticals, materials science, and agrochemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 63502-76-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,5,0 and 2 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 63502-76:
(7*6)+(6*3)+(5*5)+(4*0)+(3*2)+(2*7)+(1*6)=111
111 % 10 = 1
So 63502-76-1 is a valid CAS Registry Number.
63502-76-1Relevant academic research and scientific papers
Glorination of Pyrimidines. Part 2. Mechanistic Aspects of the Reaction of Acetyl Hypofluorite with Uracil and Cytosine Derivatives
Visser, W. M. Gerard,Herder, E. Renella,Kanter, Frans J. J. de,Herscheid D. M. Jacobus
, p. 1203 - 1208 (2007/10/02)
The reaction of acetyl hypofluorite (AcOF) with uracil, cytosine, and some N-1-substituted derivatives dissolved in either acetic acid or water has been investigated.Analysis by radio-h.p.l.c., using (18)f as a tracer, and by (1)H n.m.r. revealed that a substituent at N-1 of uracil has a remarkable effect on the stability of the intermediate 6-acetoxy-5-fluoro-5,6-dihydrouracils.In addition, it was found that these cytosine adducts rapidly deaminate in water yielding their corresponding uracil analogues.
