1489-12-9 Usage
Uses
Used in Pharmaceutical Synthesis:
2,4-bis(prop-2-en-1-yloxy)pyrimidine is utilized as a key intermediate in the synthesis of various pharmaceuticals. Its unique molecular structure allows for the creation of new drug candidates with potential therapeutic applications.
Used in Agrochemical Production:
In the agrochemical industry, 2,4-bis(prop-2-en-1-yloxy)pyrimidine is employed as a building block for the development of new agrochemicals. Its reactivity and molecular structure contribute to the formulation of effective compounds for agricultural use.
Used in Organic Compound Synthesis:
2,4-bis(prop-2-en-1-yloxy)pyrimidine is used as a versatile reagent in the synthesis of a wide range of organic compounds. Its presence in these reactions can lead to the formation of novel molecules with diverse applications.
Used in Drug Discovery and Development:
Due to its unique molecular structure and reactivity, 2,4-bis(prop-2-en-1-yloxy)pyrimidine has potential applications in the field of drug discovery and development. It may serve as a starting point for the design and synthesis of new therapeutic agents.
Used in Polymer and Plastic Manufacturing:
2,4-bis(prop-2-en-1-yloxy)pyrimidine may also have uses in the manufacturing of polymers, plastics, and other industrial materials. Its incorporation into these materials could lead to the development of new products with improved properties and performance.
Check Digit Verification of cas no
The CAS Registry Mumber 1489-12-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,8 and 9 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1489-12:
(6*1)+(5*4)+(4*8)+(3*9)+(2*1)+(1*2)=89
89 % 10 = 9
So 1489-12-9 is a valid CAS Registry Number.
1489-12-9Relevant academic research and scientific papers
Stereocontrolled synthesis of β-2'-deoxypyrimidine nucleosides via intramolecular glycosylations
Xia, Xiaoyang,Wang, Jianying,Hager, Michael W.,Sisti, Nicholas,Liotta, Dennis C.
, p. 1111 - 1114 (2007/10/03)
A pyrimidine moiety was tethered at the 3'-β-position of D-threo-furanosides. By carefully controlling the reaction conditions, pyrimidine bases can be delivered to the anomeric center to give of β-pyrimidine nucleosides in good yield and with complete stereocontrol.
Palladium-Catalyzed Rearrangements of 2-Cyclopentenyloxypyrimidines in the Preparation of Pyrimidine Carbonucleosides
Falck-Pedersen, Mette Lene,Benneche, Tore,Undheim, Kjell
, p. 72 - 79 (2007/10/02)
Allylic 2-cyclopentenyloxypyrimidines have been prepared and rearranged by Pd(0)-induced catalysis to pyrimidine carbonucleosides analogues.For acid-sensitive substrates the rearrangement was performed in the presence of a base.Assignment of regio- and stereo-chemistry is based on NMR spectroscopy.
