Tenofovir

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Identification

Molecular formula
C9H14N5O4P
CAS Number
147127-20-6
IUPAC Name
2-amino-9-(2,7-dihydroxy-2-oxo-4a,6,7,7a-tetrahydro-4H-furo[3,2-d][1,3,2]dioxaphosphinin-6-yl)-3H-purin-6-one
Molecular Weight
305.27g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.4930g/cm3
Interesting facts

Interesting Facts about 2-amino-9-(2,7-dihydroxy-2-oxo-4a,6,7,7a-tetrahydro-4H-furo[3,2-d][1,3,2]dioxaphosphinin-6-yl)-3H-purin-6-one

This fascinating compound, commonly referred to within the realm of synthetic chemistry, possesses unique structural features and functionalities. Here are some remarkable points about this chemical:

  • The compound contains a purine base, which is foundational in the structure of nucleotides, the building blocks of DNA and RNA.
  • Its complex configuration includes a phosphine oxide, indicating potential applications in medicinal chemistry, particularly in drug design and development.
  • The inclusion of multiple hydroxy groups enhances the compound’s reactivity and solubility, contributing to its versatility in various chemical reactions.
  • It features a furodioxaphosphinine ring, which is relatively rare and interesting due to its unique heterocyclic structure.
  • This compound belongs to a class of nucleobase derivatives, which are often studied for their potential role as antiviral or anticancer agents due to their ability to interact with nucleic acids.

In addition, researchers are exploring:

  • Its potential as a *bioactive agent* in cellular processes.
  • The catalytic properties it might exhibit due to the phosphorus atom’s ability to stabilize transition states during reactions.
  • The possibility of modifying its structure to enhance therapeutic efficacy or reduce side effects.

In summary, 2-amino-9-(2,7-dihydroxy-2-oxo-4a,6,7,7a-tetrahydro-4H-furo[3,2-d][1,3,2]dioxaphosphinin-6-yl)-3H-purin-6-one stands as an emblem of the intricate interplay between organic chemistry and pharmaceutical innovation, promising advancements in fields range from biochemistry to drug discovery.

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