78795-26-3 Usage
Molecular structure
The compound has a complex molecular structure, consisting of a cyclopentyl ring with a hydroxymethyl group attached to it, and a methylpyrimidine-2,4(1H,3H)-dione moiety.
Hydroxyl and methyl groups
The presence of hydroxyl and methyl groups in the molecule suggests that it may have biological activity.
Heterocyclic ring system
The compound contains a heterocyclic ring system, which is often associated with biological activity and potential pharmaceutical applications.
Potential uses
Due to its structure and potential biological activity, 1-[2-hydroxy-4-(hydroxymethyl)cyclopentyl]-5-methylpyrimidine-2,4(1H,3H)-dione may be used in pharmaceutical research and drug development.
Synthesis of new compounds
The compound can be used as a starting material for the synthesis of new organic compounds with potential medical or industrial applications.
Further research and testing
Additional research and testing would be necessary to fully understand the properties and potential uses of this chemical compound.
Molecular weight
The molecular weight of the compound is approximately 239.25 g/mol.
Solubility
The solubility of the compound in various solvents would need to be determined through experimentation, but it is likely to be soluble in polar solvents such as water and methanol due to the presence of hydroxyl groups.
Stability
The stability of the compound under different conditions (e.g., temperature, pH, light exposure) would need to be investigated to determine its suitability for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 78795-26-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,7,9 and 5 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 78795-26:
(7*7)+(6*8)+(5*7)+(4*9)+(3*5)+(2*2)+(1*6)=193
193 % 10 = 3
So 78795-26-3 is a valid CAS Registry Number.
78795-26-3Relevant academic research and scientific papers
Rapid synthesis of (±)-r-7-benzyloxymethyl-cyclopenta-cis-[4,5][1,3]-oxazolo[3,2-a] pyrimidinones versatile carbocyclic nucleoside precursors
Pérez, Nury,Gordillo, Barbara
, p. 671 - 676 (2007/10/03)
(±)-r-7-Benzyloxymethyl-cyclopenta-cis-[4,5][1,3]-oxazolo[3,2-a] pyrimidinones were synthesized in two steps from 1-hydroxymethyl-3-cyclopentene. These compounds are versatile intermediates for the synthesis of carbocyclic nucleosides. The synthesis has been accomplished by the iodofunctionalization of olefins as a method of coupling the pyrimidine bases and the carbocycle.
Synthesis of nucleosides and related compounds. XXII. Carbocyclic analogues of thymidine and related compounds from 2-azabicyclo[2.2.1]hept-5-en-3-ones
Katagiri,Nomura,Muto,Kaneko
, p. 1682 - 1688 (2007/10/02)
Reductive amido bond cleavage reaction, previously elaborated by our laboratory for the synthesis of carbocyclic ribothymidine from readily available 2-azabicyclo[2.2.1]hept-5-en-3-one, was successfully applied to the synthesis of carbocyclic analogues of thymidine and related compounds.
Carbocyclic Analogs of Thymine Nucleosides and Related 1-Substituted Thymines
Shealy, Y.Fulmer,O'Dell, C.Allen,Thorpe, Martha C.
, p. 383 - 389 (2007/10/02)
The carbocyclic analogs of thymidine (IXf), 1-β-ribofuranosylthymine (IXg), and 1-β-3'-deoxyribofuranosylthymine (IXe) were synthesized by incorporating modifications into the Shaw method of synthesizing 2,4-(1H,3H)pyrimidinediones via acryloylureas.Simpler analogs of thymine nucleosides were also prepared by this method.The carbocyclic analog of thymidine displayed modest activity against Leukemia L1210 in vivo.It differs from a compound prepared previously by a Prins reaction.
