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Adenosine monophosphate

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Identification
Molecular formula
C10H14N5O7P
CAS number
61-19-8
IUPAC name
(5-amino-3,4-dihydroxy-tetrahydrofuran-2-yl)methyl dihydrogen phosphate
State
State

At room temperature, adenosine monophosphate is a solid.

Melting point (Celsius)
178.00
Melting point (Kelvin)
451.00
Boiling point (Celsius)
390.00
Boiling point (Kelvin)
663.00
General information
Molecular weight
347.22g/mol
Molar mass
347.2210g/mol
Density
2.5400g/cm3
Appearence

Adenosine monophosphate typically appears as a white crystalline powder. It is a nucleotide commonly found in food supplements and is involved in numerous biochemical processes.

Comment on solubility

Solubility of (5-amino-3,4-dihydroxy-tetrahydrofuran-2-yl)methyl dihydrogen phosphate

The solubility of the compound (5-amino-3,4-dihydroxy-tetrahydrofuran-2-yl)methyl dihydrogen phosphate, with the chemical formula C10H14N5O7P, can be characterized as follows:

  • Water Solubility: This compound is generally expected to be soluble in water due to the presence of multiple hydroxyl (–OH) groups and phosphate (–PO4) functional groups, which can interact favorably with water molecules.
  • Organic Solvents: Solubility in organic solvents is likely limited, as the hydrophilic nature of the functional groups may hinder interaction with nonpolar solvents.
  • Temperature Dependence: The solubility may increase with temperature, a common trend for many organic compounds, although specific data for this compound is required for confirmation.

In summary, it can be stated that:

  1. The compound is likely to exhibit good solubility in aqueous environments.
  2. Limited solubility in nonpolar solvents is anticipated.
  3. Temperature and pH can play significant roles in affecting solubility.

Understanding the solubility of this compound can provide crucial insights into its reactivity and applications in various chemical and biological contexts.

Interesting facts

Interesting Facts about (5-amino-3,4-dihydroxy-tetrahydrofuran-2-yl)methyl dihydrogen phosphate

This compound, often abbreviated in research contexts, boasts a fascinating structure that intertwines both organic and inorganic chemistry. Here are some intriguing points that highlight its significance:

  • Dual Nature: This molecule represents a blend of amino sugars and phosphate groups, bridging the gap between carbohydrates and biochemistry.
  • Biological Relevance: It is closely related to nucleotides and plays a role in various biochemical pathways, such as in nucleotide metabolism and signal transduction.
  • Phosphate Group Advantage: The presence of the dihydrogen phosphate group facilitates its interaction with enzymes, making it a potential candidate for studying enzymatic activity.
  • Research Potential: Compounds like this are often explored for their applications in drug design, especially in the field of pharmaceuticals where modifying such molecules can enhance therapeutic effects.
  • Functional Group Importance: The amino and hydroxy groups create opportunities for hydrogen bonding, which can significantly influence the compound’s solubility and biological interactions.

Moreover, “the study of such compounds not only furthers our understanding of biochemical interactions but also opens doors to novel applications in medicine and biotechnology.” There is growing interest in how derivatives of this compound could serve in the development of efficient drug delivery systems or even as therapeutic agents themselves.

As the scientific community continues to explore the vast landscape of chemical compounds, (5-amino-3,4-dihydroxy-tetrahydrofuran-2-yl)methyl dihydrogen phosphate stands out as a compelling subject for further research and discovery.

Synonyms
Phosphoribosylamine
5-phospho-b-D-Ribosylaminium(1-)
(5-amino-3,4-dihydroxyoxolan-2-yl)methyl dihydrogen phosphate
SCHEMBL2129355
L000658
Q3079150