Xanthosine
Structural Formula Vector Image
Title: Xanthosine
CAS Registry Number: 146-80-5
Additional Names: Xanthine riboside; 9-b-D-ribofuranosyl xanthine; 9-b-D-ribofuranosyl-9H-purine-2,6-diol; 9-b-D-ribofuranosyl-9H-purine-2,6-(1H,3H)-dione
Molecular Formula: C10H12N4O6
Molecular Weight: 284.23
Percent Composition: C 42.26%, H 4.26%, N 19.71%, O 33.77%
Literature References: Prepd from guanosine by treatment with sodium nitrite and acetic acid: Levene, Jacobs, Ber. 43, 3163 (1910); Gulland, Macrae, J. Chem. Soc. 1933, 662. Synthesis: Howard et al., ibid. 1949, 232. Biosynthesis: Magasanik, Brooke, J. Biol. Chem. 206, 83 (1954); Korn, Buchanan, ibid. 217, 183 (1955); Bolis et al., ibid. 219, 917 (1956).
 
Derivative Type: Dihydrate
Properties: Long prisms from water. Anhydr felted clusters (warts) from alc. Dec on heating, no distinct melting range. [a]D30 -51.2° (p = 8 in 0.3N NaOH). uv max: 253 nm (e 8.790). aM (molar absorbancy): 11.4´103 at 248.5 nm in water at pH 8.0. Sparingly sol in cold water; freely sol in hot water; sol in hot dil alcohol. Easily hydrolyzed by mineral acids.
Optical Rotation: [a]D30 -51.2° (p = 8 in 0.3N NaOH)
Absorption maximum: uv max: 253 nm (e 8.790)

Other Monographs:
SpandexLithium Bromide3-HydroxycamphorAluminum Stearate
CargutocinAconitum FeroxIsosorbideCyclopentobarbital
TriphenylmethaneHaloxazolamRifabutinCreosote, Wood
AmitonTelavancinPerchloric AcidAlizarin
©2006-2023 DrugFuture->Chemical Index Database