59464-15-2 Usage
Uses
Used in Pharmaceutical Industry:
1-(2-amino-6-oxo-1,6-dihydropyrimidin-5-yl)-1,4-anhydropentitol is used as a potential pharmaceutical compound for its possible incorporation into biologically active molecules. The presence of the dihydropyrimidine ring, which is common in various pharmaceutical agents, suggests that 1-(2-amino-6-oxo-1,6-dihydropyrimidin-5-yl)-1,4-anhydropentitol could be a valuable building block for the development of new drugs.
Used in Organic Synthesis:
1-(2-amino-6-oxo-1,6-dihydropyrimidin-5-yl)-1,4-anhydropentitol is used as a synthetic building block for its anhydride group, which could be exploited in organic synthesis reactions to create a variety of complex molecules with potential applications in different industries, including pharmaceuticals, materials science, and agrochemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 59464-15-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,4,6 and 4 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 59464-15:
(7*5)+(6*9)+(5*4)+(4*6)+(3*4)+(2*1)+(1*5)=152
152 % 10 = 2
So 59464-15-2 is a valid CAS Registry Number.
59464-15-2Relevant academic research and scientific papers
A stereocontrolled total synthesis of C-nucleosides
Sato,Hayakawa,Noyori
, p. 2515 - 2525 (2007/10/02)
A stereocontrolled, general synthesis of chiral C-nucleosides has been achieved through a common lactonic C- beta -glycoside intermediate which is readily obtainable from non-carbohydrate materials. The optically pure lactone having the natural D configuration is obtained through optical resolution of the seco acid by the Pirkle's method followed by relactonization. alpha -Aminomethylenation of the lactone with t-C//4H//9OCH left bracket N(CH//3 )//2 right bracket //2 yields 2-(2,3-0-isopropylidene- beta -D-ribofuranosyl)-2-(dimethylaminomethylene)acetic acid lactone, which undergoes base-assisted condensation with urea followed by deprotection to furnish naturally occurring pseudouridine. Analogously, construction of heterocycles using thiourea and guanidine converts the aminomethylene lactone to unnatural pyrimidine C-nucelosides, 2-thiopseudouridine and pseudoisocytidine, respectively.
