65926-38-7 Usage
Chemical class
Pyrimidines Heterocyclic aromatic organic compounds with a pyrimidine ring structure.
Derivative
Heptofuranuronic acid A sugar acid that forms the backbone of some complex carbohydrates.
Pyrimidine ring
A six-membered heterocyclic ring with four carbon atoms and two nitrogen atoms.
Dioxo group
Two oxygen atoms double-bonded to adjacent carbon atoms in the pyrimidine ring.
Furanose ring
A five-membered ring structure containing one oxygen atom and four carbon atoms.
Potential applications
Medicinal chemistry and drug discovery Due to its structural features and potential interactions with biological molecules.
Research status
Further research is needed to fully understand its properties and potential uses.
Biological activities
The presence of a furanose ring in the molecule may contribute to unique properties and potential biological activities, which are yet to be explored.
Molecular weight
Approximately 256.22 g/mol The mass of one mole of the compound.
Solubility
Unknown Further research is needed to determine the solubility of the compound in various solvents.
Stability
Unknown Further research is needed to determine the stability of the compound under different conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 65926-38-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,9,2 and 6 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 65926-38:
(7*6)+(6*5)+(5*9)+(4*2)+(3*6)+(2*3)+(1*8)=157
157 % 10 = 7
So 65926-38-7 is a valid CAS Registry Number.
65926-38-7Relevant academic research and scientific papers
Diazomethyl Ketone Derivatives of Pyrimidine Nucleosides
Montgomery, John A.,Thomas, H. Jeanette
, p. 594 - 598 (2007/10/02)
1,5,6,8-Tetradeoxy-8-diazo-β-D-erythro-7-octulofuranosylthymine (20) and 5,6,8-trideoxy-8-diazo-β-D-ribo-7-octulofuranosyluracil (31), pyrimidine nucleosides containing the reactive diazomethyl ketone function, were prepared from thymidine and uridine via
