59090-35-6 Usage
Uses
Used in Pharmaceutical and Agrochemical Production:
5-prop-2-enyl-1H-pyrimidine-2,4-dione is used as an intermediate in the production of pharmaceutical and agrochemical products. Its unique structure allows it to be a key component in the synthesis of various compounds with therapeutic and pesticidal properties.
Used in Organic Synthesis:
In the field of organic synthesis, 5-prop-2-enyl-1H-pyrimidine-2,4-dione is utilized as a building block for the creation of more complex molecules. Its reactivity and functional groups make it a valuable precursor in the development of new chemical entities.
Used in Pharmaceutical Research:
5-prop-2-enyl-1H-pyrimidine-2,4-dione is used as a research compound in pharmaceutical studies. Scientists explore its potential applications, including its possible role in the development of new drugs and therapies.
Used in Antifungal Applications:
5-prop-2-enyl-1H-pyrimidine-2,4-dione has been studied for its potential antifungal properties. It may be used as an active ingredient in antifungal agents to combat fungal infections.
Overall, 5-prop-2-enyl-1H-pyrimidine-2,4-dione is a multifaceted chemical with applications spanning across various industries, from pharmaceuticals and agrochemicals to organic synthesis and research. Its versatility and potential for further development make it an important compound in the field of chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 59090-35-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,0,9 and 0 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 59090-35:
(7*5)+(6*9)+(5*0)+(4*9)+(3*0)+(2*3)+(1*5)=136
136 % 10 = 6
So 59090-35-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H8N2O2/c1-2-3-5-4-8-7(11)9-6(5)10/h2,4H,1,3H2,(H2,8,9,10,11)
59090-35-6Relevant academic research and scientific papers
Functionalization of unprotected uracil derivatives using the halogen - Magnesium exchange
Kopp, Felix,Knoechel, Paul
, p. 1639 - 1641 (2008/02/02)
The reaction of commercially available 5-iodouracil with 2 equiv of MeMgCl in the presence of LiCl, followed by the addition of i-PrMgCl-LiCl, provides the corresponding trimagnesiated species, which reacts with various electrophiles to give selectively 5
Synthesis and anti-herpes virus activity of 2'-deoxy-4'-thiopyrimidine nucleosides
Rahim,Trivedi,Bogunovic-Batchelor,Hardy,Mills,Selway,Snowden,Littler,Coe,Basnak,Whale,Walker
, p. 789 - 795 (2007/10/03)
A series of 5-substituted 2'-deoxy-4'-thiopyrimidine nucleosides was synthesized and evaluated as potential antiviral agents. A number of analogues such as 2'-deoxy-5-propyl-4'-thiouridine (3ii), 2'-deoxy-5- isopropyl-4'-thiouridine (3iii), 5-cyclopropyl-
Antiviral pyrimidine nucleosides
-
, (2008/06/13)
Pyrimidine 4'-thionucleosides of the formula I STR1 wherein Y is hydroxy or amino, and X is chloro, bromo, iodo, trifluoromethyl, C2-6 alkyl, C2-6 alkenyl, C2-6 haloalkenyl or C2-6 alkynyl and physiologically functional derivatives thereof. These compounds have utility as anti-vital agents.
