2′-Deoxyinosine

• Catalog No.: D5287
• CAS Number: 890-38-0
• M. F.: C10H12N4O4
• M. W.: 252.22668
• Purity: ≥98%

SYNONYMS

• IUPAC name: 9-[(2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-6,9-dihydro-1H-purin-6-one
• IUPAC Traditional name: 2'-deoxyinosine
• Synonyms: 9-(2-Deoxy-β-D-ribofuranosyl)hypoxanthine

DATABASE IDS

• CAS Number: 890-38-0
• Beilstein Number: 33517
• MDL Number: MFCD00005762
• PubChem SID: 24893935
• EC Number: 212-964-1

PROPERTIES

• Empirical Formula (Hill Notation): C10H12N4O4
• Impurities: inosine, essentially free
• Purity: ≥98%
• Personal Protective Equipment: Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
• Storage Temperature: -20°C
• German water hazard class: 3

DETAILS

Description (English)

Application
2′-Deoxyinosine is a nucleoside composed of hypoxanthine attached to 2′-deoxyribose via a β-N9-glycosidic bond. 2′-Deoxyinosine in DNA can arise from deamination of adenosine. 2′-deoxyinsine can be used as a model compound to study the chemistry of adduct formation and radical chemistry that may affect DNA structures. 2′-Deoxyinosine is used to produce hybridization-sensitive fluorescent DNA probes with self-avoidance ability.

Description (简体中文)

Application
2′-Deoxyinosine is a nucleoside composed of hypoxanthine attached to 2′-deoxyribose via a β-N9-glycosidic bond. 2′-Deoxyinosine in DNA can arise from deamination of adenosine. 2′-deoxyinsine can be used as a model compound to study the chemistry of adduct formation and radical chemistry that may affect DNA structures. 2′-Deoxyinosine is used to produce hybridization-sensitive fluorescent DNA probes with self-avoidance ability.