Raman spectral studies of nucleic acids and related molecules. I. Ribonucleic acid derivatives was written by Lord, Richard C.;Thomas, George J. Jr.. And the article was included in Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy in 1967.Computed Properties of C9H12N3Na2O8P This article mentions the following:
Raman spectra of the commonly occurring purine and pyrimidine derivatives of ribonucleic acid are reported. The free bases, nucleosides, 5′-mononucleotides, and related alkyl derivatives have been examined in aqueous solutions over wide pH and pD ranges as well as in the solid state. The ir spectra of the solids, some not previously reported, are also included. The spectra are discussed in terms of the changes in mol. structure produced by changes in pH, pD, and state of aggregation. This discussion is intended to serve as a basis for further investigation of intermol. interactions of nucleic acid derivatives in aqueous solution The Raman effect appears to offer much promise for this kind of study. 26 references. In the experiment, the researchers used many compounds, for example, Sodium ((2R,3S,4R,5R)-5-(4-amino-2-oxopyrimidin-1(2H)-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl phosphate (cas: 6757-06-8Computed Properties of C9H12N3Na2O8P).
Sodium ((2R,3S,4R,5R)-5-(4-amino-2-oxopyrimidin-1(2H)-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl phosphate (cas: 6757-06-8) belongs to tetrahydrofuran derivatives. Solid acid catalysis, and the advantages often associated with their use, have been proved equally efficient for the synthesis of tetrahydrofurans or furans. Tetrahydrofuran can also be produced, or synthesised, via catalytic hydrogenation of furan. This process involves converting certain sugars into THF by digesting to furfural. An alternative to this method is the catalytic hydrogenation of furan with a nickel catalyst.Computed Properties of C9H12N3Na2O8P
Referemce:
Tetrahydrofuran – Wikipedia,
Tetrahydrofuran | (CH2)3CH2O – PubChem