Home > Name List By 9 > 9-[(2R,3R,4S,5R)-3, 4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-3H-purin-6-one Germany

CAS No 58-63-9 , 9-[(2R,3R,4S,5R)-3,
4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-3H-purin-6-one Search by region : Germany

  • Name: 9-[(2R,3R,4S,5R)-3,
    4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-3H-purin-6-one
  • Synonyms: Selfer; Pantholic-L; Trophicardyl; Atorel; Panholic-L; beta-Inosine; Ribonosine;Hypoxanthosine; Oxiamin;9-[(2R,3R,4S,5R)-3,
    4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-3H-purin-6-one;
  • CAS Registry Number:
  • Melting Point: 212-213 ºC
  • Density: 2.08 g/cm3
  • Refractive index: -52 ° (C=1, H2O)
  • Alpha: -49.2 º (C=1,H2O 18 ºC)
  • Water Solubility: 2.1 G/100 ML (20 ºC)
  • Safety Statements: Moderately toxic by intraperitoneal route. Mutation data reported. When heated to decomposition it emits toxic fumes of NOx.
  • Hazard Symbols: Xi
  • EINECS: 200-390-4
  • Molecular Weight: 268.22608
  • InchiKey: UGQMRVRMYYASKQ-KQYNXXCUSA-N
  • InChI: InChI=1S/C10H12N4O5/c15-1-4-6(16)7(17)10(19-4)14-3-13-5-8(14)11-2-12-9
    (5)18/h2-4,6-7,10,15-17H,1H2,(H,11,12,18)/t4-,6-,7-,10-/m1/s1
  • Risk Statements: S24/25
  • Molecular Formula: C10H12N4O5
  • Molecular Structure:CAS No:58-63-9 9-[(2R,3R,4S,5R)-3,<br />4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-3H-purin-6-one

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1/1
References of 9-[(2R,3R,4S,5R)-3,
4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-3H-purin-6-one
Title: Inosine
CAS Registry Number: 58-63-9
Synonyms: Hypoxanthine riboside; 9-b-D-ribofuranosylhypoxanthine; hypoxanthosine
Trademarks: Inosie (Morishita); Oxiamine (Made); Ribonosine (Toyo Jozo); Trophicardyl
Molecular Formula: C10H12N4O5
Molecular Weight: 268.23
Percent Composition: C 44.78%, H 4.51%, N 20.89%, O 29.82%
Literature References: In meat and meat extracts, in sugar beets. Prepd from adenosine by incubation with purified adenosine deaminase from intestine: Kalckar, J. Biol. Chem. 167, 445 (1947); also by the action of sodium nitrite and acetic acid on adenosine: Levene, Jacobs, Ber. 43, 3161 (1910); by the use of barium nitrite and H2SO4: Reiff et al., US 3049536 (1962 to Zellstoff-Fabrik Waldhof). Fermentation method: Motozaki et al., US 3111459 (1963 to Ajinomoto). Structure: Bredereck, Ber. 66, 198 (1933); Z. Physiol. Chem. 223, 61 (1934); Gulland, Holiday, J. Chem. Soc. 1936, 765.
 
Derivative Type: Dihydrate
Properties: Long rectangular plates from water, mp 90°. Anhydrous needles from 80% alc, dec 218° (rapid heating). [a]D18 -49.2° (c = 0.9 in H2O). [a]20white -73° (0.5 g + 2 ml N NaOH + 3 ml H2O). 100 ml of the satd water soln at 20° contain 1.6 g inosine. Absorption spectrum: Kalckar, loc. cit. uv max (pH 6.0): 248.5 nm (e 12200). Boiling with 0.1N H2SO4 yields hypoxanthin and D-ribose.
Melting point: mp 90°
Optical Rotation: [a]D18 -49.2° (c = 0.9 in H2O); [a]20white -73° (0.5 g + 2 ml N NaOH + 3 ml H2O)
Absorption maximum: uv max (pH 6.0): 248.5 nm (e 12200)
 
Therap-Cat: Activates cellular functions.