120889-35-2 Usage
Uses
Used in Pharmaceutical Industry:
2,4(1H,3H)-Pyrimidinedione, 1-ethyl-5-fluorois utilized as a pharmaceutical intermediate for the synthesis of antiviral and antitumor drugs. Its unique structure and properties make it a valuable component in the development of medications targeting various viral infections and cancerous conditions.
Used in Autoimmune and Inflammatory Disorder Treatment:
2,4(1H,3H)-Pyrimidinedione, 1-ethyl-5-fluorois also recognized for its potential use in treating autoimmune diseases and inflammatory disorders. Its application in this field is attributed to its capacity to modulate immune responses and reduce inflammation, offering a promising therapeutic option for patients suffering from such conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 120889-35-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,8,8 and 9 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 120889-35:
(8*1)+(7*2)+(6*0)+(5*8)+(4*8)+(3*9)+(2*3)+(1*5)=132
132 % 10 = 2
So 120889-35-2 is a valid CAS Registry Number.
120889-35-2Relevant academic research and scientific papers
The photocycloaddition reactions of uridine and related compounds with 2,3-dimethyl-2-butene
Ishikawa,Itoh,Takayanagi,Oshima,Kawahara,Mizuno,Ogura
, p. 1922 - 1930 (2007/10/02)
The photochemical reactions of uracil and 5-fluorouracil derivatives with simple alkenes have been investigated. Photocycloaddition of uracil or 5-fluorouracil derivatives and 2,3-dimethyl-2-butene in acetone gave an enantiomeric mixture of cross cycloadducts (4, 7) in moderate yields. Under similar conditions, diastereomers of 4-substituted 7,7,8,8-tetramethyl-cis-2,4-diazabicyclo[4.2.0]octane-3,5-dione nucleosides (14-17) were formed from uridine or 5-fluorouridine derivatives in good yields. The structures and stereochemistry of these cycloadducts of the nucleoside series were elucidated on the basis of the proton nuclear magnetic resonance spectra and X-ray crystallographic analysis.
