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CAS 1956-30-5

:

Uridine, 2′-deoxy-5-iodo-, 3′,5′-diacetate

Description:
Uridine, 2′-deoxy-5-iodo-, 3′,5′-diacetate, with the CAS number 1956-30-5, is a modified nucleoside derivative of uridine. This compound features a deoxy ribose sugar, which means it lacks an oxygen atom at the 2′ position compared to ribonucleosides. The presence of iodine at the 5′ position introduces a halogen, which can influence the compound's reactivity and biological activity. The diacetate groups at the 3′ and 5′ positions serve as protective acetyl groups, which can enhance the compound's stability and solubility in organic solvents. This modification is often utilized in biochemical applications, including nucleic acid synthesis and as a building block in the development of nucleoside analogs. The compound's structure allows it to participate in various biochemical processes, potentially affecting cellular functions and interactions. Overall, its unique characteristics make it a valuable compound in both research and therapeutic contexts.
Formula:C13H15IN2O7
InChI:InChI=1S/C13H15IN2O7/c1-6(17)21-5-10-9(22-7(2)18)3-11(23-10)16-4-8(14)12(19)15-13(16)20/h4,9-11H,3,5H2,1-2H3,(H,15,19,20)/t9-,10+,11+/m0/s1
InChI key:InChIKey=LVDYIZDWXVFTQG-HBNTYKKESA-N
SMILES:O=C1N([C@@H]2O[C@H](COC(C)=O)[C@@H](OC(C)=O)C2)C=C(I)C(=O)N1
Synonyms:
  • 1-(3,5-di-O-acetyl-2-deoxy-5-C-iodopentofuranosyl)pyrimidine-2,4(1H,3H)-dione
  • 3',5'-Di-O-Acetyl-5-Iodo-2'-Deoxyuridine
  • 3',5'-Diacetyl-5-Iodo-2'-Deoxyuridine
  • 3',5'-di-O-acetyl-2'-deoxy-5-iodouridine
  • 3′,5′-Di-O-acetyl-5-iodo-2′-deoxyuridine
  • Uridine, 2′-deoxy-5-iodo-, 3′,5′-diacetate
  • 2'-Deoxy-5-iodouridine 3',5'-diacetate
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