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Ibotenic acid

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Identification
Molecular formula
C5H6ClNO3
CAS number
2552-55-8
IUPAC name
2-amino-2-(3-chloro-4,5-dihydroisoxazol-5-yl)acetic acid
State
State

Ibotenic acid is generally in the solid state at room temperature, usually found as a crystalline powder.

Melting point (Celsius)
151.00
Melting point (Kelvin)
424.00
Boiling point (Celsius)
257.00
Boiling point (Kelvin)
530.00
General information
Molecular weight
158.06g/mol
Molar mass
158.0550g/mol
Density
1.8220g/cm3
Appearence

Ibotenic acid typically appears as a white powder.

Comment on solubility

Solubility of 2-amino-2-(3-chloro-4,5-dihydroisoxazol-5-yl)acetic acid

The compound 2-amino-2-(3-chloro-4,5-dihydroisoxazol-5-yl)acetic acid, with the chemical formula C5H6ClNO3, exhibits interesting solubility characteristics in various solvents. The solubility of this compound can be influenced by several factors:

  • Polarity of the Solvent: Due to the presence of both acidic and functional amine groups, the compound has a relatively polar nature. As a result, it shows a greater solubility in polar solvents like water compared to non-polar solvents.
  • Temperature: Increasing the temperature generally enhances solubility for most compounds, including this one, due to the higher kinetic energy which aids in breaking intermolecular forces.
  • pH Levels: The solubility may vary with changes in pH, particularly because it can form ionic species in different acid-base environments, impacting its solubility significantly.

In summary, one can expect that 2-amino-2-(3-chloro-4,5-dihydroisoxazol-5-yl)acetic acid is likely to be readily soluble in polar solvents, especially under elevated temperatures and appropriate pH conditions. This combined understanding of its solubility profile helps in predicting its behavior in various chemical environments.

Interesting facts

Interesting Facts about 2-amino-2-(3-chloro-4,5-dihydroisoxazol-5-yl)acetic acid

The compound 2-amino-2-(3-chloro-4,5-dihydroisoxazol-5-yl)acetic acid is a fascinating member of the amino acid family due to its unique structural features and diverse applications. Here are some intriguing aspects of this compound:

  • Biological Relevance: This compound has been studied for its potential therapeutic effects, particularly within neurological contexts. The presence of the isoxazole ring may influence its function in modulation of neurotransmitter activity.
  • Synthesis Techniques: Chemists employ various methods to synthesize this compound, including the use of specific reagents that facilitate the formation of the amino acid structure and the chlorinated isoxazole ring.
  • Research Applications: 2-amino-2-(3-chloro-4,5-dihydroisoxazol-5-yl)acetic acid has caught the attention of researchers aiming to develop new pharmaceuticals, especially for diseases like epilepsy and anxiety disorders.
  • Functional Versatility: The compound can act as a building block for more complex molecules, showcasing its versatility in organic synthesis, which often leads to the discovery of novel compounds.
  • Chirality: As an amino acid, this compound possesses chirality, which means it can exist in different stereoisomers. The specific enantiomer used can have significant effects on biological activity.

In summary, 2-amino-2-(3-chloro-4,5-dihydroisoxazol-5-yl)acetic acid is not just another amino acid; its unique characteristics and potential applications in medicinal chemistry make it a subject of ongoing scientific inquiry. As the famous chemist Linus Pauling once said, "The best way to have a good idea is to have a lot of ideas." This compound may very well be one of those ideas leading to innovative breakthroughs in the future.

Synonyms
52583-41-2
5-Isoxazoleacetic acid, alpha-amino-3-chloro-4,5-dihydro-
2-amino-2-(3-chloro-4,5-dihydro-1,2-oxazol-5-yl)acetic acid
2-amino-2-(3-chloro-4,5-dihydroisoxazol-5-yl)acetic acid
alpha-Amino-3-chloro-4,5-dihydro-5-isoxazoleacetic acid
amino(3-chloro-4,5-dihydro-1,2-oxazol-5-yl)acetic acid
AT-125;U-42126
MLS000028629
SCHEMBL1873697
(2S)-2-amino-2-[(5S)-3-chloro-4,5-dihydroisoxazol-5-yl]acetic acid
CHEMBL1337040
BCBcMAP01_000236
DTXSID80860588
AKOS006237405
SMP1_000002
AC-31550
SMR000058744
DB-070274
SR-01000721919
SR-01000721919-3
Q26841004
5-Isoxazoleacetic acid,alpha-amino-3-chloro-4,5-dihydro-
2-azanyl-2-(3-chloranyl-4,5-dihydro-1,2-oxazol-5-yl)ethanoic acid