5-Iodouridine monohydrate

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Identification

Molecular formula
C9H11IN2O6
CAS Number
320-40-1
IUPAC Name
1-[(2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl]-5-iodo-pyrimidine-2,4-dione;hydrate
Molecular Weight
384.10g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
2.3200g/cm3
Synonyms
IDOXURIDINE MONOHYDRATE
Interesting facts

Interesting Facts about 1-[(2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl]-5-iodo-pyrimidine-2,4-dione; hydrate

This intriguing compound, often referred to in scientific literature due to its potential applications in pharmaceuticals, presents a fascinating structure that intertwines both carbohydrate and heterocyclic chemistry. Here are some noteworthy points:

  • Structural Complexity: The compound exhibits a unique combination of a pyrimidine ring and a tetrahydrofuran structure. This fusion of structural elements showcases the versatility of organic chemistry in creating complex molecules.
  • Biological Relevance: Compounds related to pyrimidines are often explored for their biological activity. They serve as essential building blocks in the synthesis of nucleic acids and have significant roles in cellular processes.
  • Hydroxy Functionality: The presence of hydroxy groups within its structure can enhance interactions with biological targets, making this compound a candidate for further exploration in medicinal chemistry.
  • Popularity in Research: As scientists search for new therapeutic agents, this compound may emerge as a focus due to its potential anti-viral or anti-cancer properties, aligning with the ongoing demand for innovative treatments.
  • Quote from a Chemist: "Nature's creativity in molecular design is unparalleled. Each compound holds a story waiting to be unraveled, and this one is no exception!"

In summary, 1-[(2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl]-5-iodo-pyrimidine-2,4-dione; hydrate is not just a molecule; it represents a crossroads of various scientific fields, highlighting the importance of interdisciplinary approaches in modern chemistry.

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