75500-03-7 Usage
Uses
Used in Organic Synthesis:
1,3-Di(benzyloxymethyl)-5-fluorouracil is used as an intermediate in the synthesis of various organic compounds, particularly those with potential pharmaceutical applications. Its unique structure allows for further functionalization and modification, making it a valuable building block in the development of new drugs and chemical entities.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 1,3-Di(benzyloxymethyl)-5-fluorouracil is used as a starting material for the development of novel therapeutic agents. Its structural similarity to 5-fluorouracil, a widely used anticancer drug, makes it an attractive candidate for the design of new anticancer drugs with potentially improved efficacy and reduced side effects.
Used in Drug Delivery Systems:
Similar to gallotannin, 1,3-Di(benzyloxymethyl)-5-fluorouracil can also be employed in the development of drug delivery systems. These systems aim to improve the bioavailability, targeting, and overall therapeutic outcomes of the compound by encapsulating it within nanoparticles, liposomes, or other carriers.
Check Digit Verification of cas no
The CAS Registry Mumber 75500-03-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,5,0 and 0 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 75500-03:
(7*7)+(6*5)+(5*5)+(4*0)+(3*0)+(2*0)+(1*3)=107
107 % 10 = 7
So 75500-03-7 is a valid CAS Registry Number.
InChI:InChI=1/C20H19FN2O4/c21-18-11-22(14-26-12-16-7-3-1-4-8-16)20(25)23(19(18)24)15-27-13-17-9-5-2-6-10-17/h1-11H,12-15H2
75500-03-7Relevant academic research and scientific papers
A new synthesis of n-blocked dihydrouracil and dihydroorotic acid derivatives using lithium tri-sec-butyl borohydride as reducing agent
Hannon, Stephen J.,Kundu, Nitya G.,Hertzberg, Robert P.,Bhatt, Ram S.,Heidelberger, Charles
, p. 1105 - 1108 (2007/10/02)
1,3-Di-N-substituted uracil and its derivatives have been reduced with lithium-tri-sec-butyl borohydride to the corresponding 5,6-dihydro compounds in excellent yields. Alkylation of 5-position of uracil is also very conveniently accomplished.
