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ATPO

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Identification
Molecular formula
C10H14N2O4
CAS number
72818-94-5
IUPAC name
2-amino-3-(5-tert-butyl-3-oxo-isoxazol-4-yl)propanoic acid
State
State

At room temperature, ATPO is usually found in a solid state. It is a stable compound under normal conditions of use and storage.

Melting point (Celsius)
121.00
Melting point (Kelvin)
394.00
Boiling point (Celsius)
285.00
Boiling point (Kelvin)
558.00
General information
Molecular weight
212.23g/mol
Molar mass
212.2300g/mol
Density
1.2500g/cm3
Appearence

ATPO is a crystalline solid that is typically colorless or white. It may appear as a powder or as crystalline granules depending on the specific conditions of preparation.

Comment on solubility

Solubility of 2-amino-3-(5-tert-butyl-3-oxo-isoxazol-4-yl)propanoic acid

The solubility of 2-amino-3-(5-tert-butyl-3-oxo-isoxazol-4-yl)propanoic acid, with the chemical formula C10H14N2O4, is influenced by several factors, including its molecular structure and functional groups. Understanding its solubility can provide insights into its potential applications and behavior in various environments.

Key Aspects of Solubility:

  • Polar Functional Groups: The presence of polar functional groups, such as the carboxylic acid (-COOH) and amino (-NH2) groups, typically enhances the solubility of the compound in polar solvents, particularly water.
  • Log P Value: The Log P (partition coefficient) can indicate hydrophilicity versus lipophilicity, influencing solubility in organic versus aqueous media.
  • Hydrogen Bonding: The ability to form hydrogen bonds with solvent molecules can significantly increase solubility. Compounds that are capable of interacting through hydrogen bonding generally have better solubility profiles.
  • Chain Length and Branching: With the inclusion of a tert-butyl group, steric hindrance may play a role, potentially affecting solubility in certain solvents.

General Observations:

Given the structure of 2-amino-3-(5-tert-butyl-3-oxo-isoxazol-4-yl)propanoic acid, one might anticipate that:

  • It should exhibit good solubility in aqueous environments due to the polar nature of its functional groups.
  • Its solubility may vary with changes in pH, particularly as the carboxylic acid can donate a proton under basic conditions, enhancing solubility.

In summary, while definitive solubility data may vary, the structural attributes of this compound strongly suggest that it has a reasonable solubility profile in polar solvents, making it suitable for various applications in chemical formulations and biological systems.

Interesting facts

Interesting Facts about 2-amino-3-(5-tert-butyl-3-oxo-isoxazol-4-yl)propanoic acid

2-amino-3-(5-tert-butyl-3-oxo-isoxazol-4-yl)propanoic acid, often abbreviated as a complex organic molecule, stands out in the realm of chemical compounds due to its fascinating structure and potential applications in various fields.

Structural Insights

This compound features:

  • Amino group: A vital part of amino acids, influencing protein synthesis and metabolism.
  • Isoxazole ring: A five-membered heterocyclic compound that grants unique reactivity patterns and biological activities.
  • Bulky tert-butyl group: This functional group adds steric hindrance, which can enhance selectivity in chemical reactions.

Biological Importance

Research has shown that derivatives of this compound may exhibit:

  • Neuroprotective properties: Compounds similar in structure have been studied for their effects on various neurodegenerative diseases.
  • Antimicrobial activity: The unique combination of functional groups may play a role in combating bacterial and fungal infections.

Applications in Chemistry

In the field of synthetic chemistry, this compound's unique structure opens doors for:

  • Drug Design: A focus of study for potentially developing new therapeutic agents.
  • Material Science: Exploring its applications in creating novel materials with specific properties.

As one of the numerous compounds in organic chemistry, 2-amino-3-(5-tert-butyl-3-oxo-isoxazol-4-yl)propanoic acid exemplifies the intricate relationship between molecular structure and function. Its study continues to inspire chemists to unravel more about its capabilities and applications in science!

Synonyms
ATPA
140158-50-5
(R,S)-ATPA
2-Amino-3-(3-hydroxy-5-tert-butylisoxazol-4-yl)propionic acid
alpha-Amino-5-(1,1-dimethylethyl)-2,3-dihydro-3-oxo-4-isoxazolepropanoic acid
Atpa-tert
(RS)-2-Amino-3-(3-hydroxy-5-tert-butylisoxazol-4-yl)propanoic acid
2-amino-3-(5-tert-butyl-3-oxo-1,2-oxazol-4-yl)propanoic acid
83654-14-2
2005454-39-5
N-[[[(1S)-3-Amino-1-[3-(3R)-3-morpholinyl-1,2,4-oxadiazol-5-yl]-3-oxopropyl]amino]carbonyl]-L-threonine
SR-01000075419
alpha-Amino-3-hydroxy-5-tert-butyl-4-isoxazolepropionate
ATPA, solid
4-Isoxazolepropanoic acid, alpha-amino-5-(1,1-dimethylethyl)-2,3-dihydro-3-oxo-
MLS002153206
CHEMBL113180
SCHEMBL4311779
SCHEMBL13957587
BDBM85741
CHEBI:91806
DTXSID10930723
HMS2231A09
HMS3267K10
HMS3371I04
HMS3412I09
HMS3676I09
NSC_2253
AKOS024456386
AKOS030530587
DA-50783
MS-23293
SMR001230685
HY-101261
CAS_140158-50-5
CS-0021056
G13075
SR-01000075419-1
SR-01000075419-3
3-(5-tert-butyl-3-hydroxy-1,2-oxazol-4-yl)alanine
BRD-A65145453-001-02-0
BRD-A65145453-001-06-1
Q12062353
2-amino-3-(5-tert-butyl-3-hydroxyisoxazol-4-yl)propanoic acid
(R,S)-alpha-Amino-3-hydroxy-5-t-butyl-4-isoxazolepropionic acid
(rs)-2-amino-3-(3-hydroxy-5-t-butylisoxazol-4-yl)propanoic acid
2-Amino-3-(3-hydroxy-5-tert-bu-tylisoxazol-4-yl)propanoic acid
2-amino-3-(5-(tert-butyl)-3-hydroxyisoxazol-4-yl)propanoic acid
2-Amino-3-(5-(tert-butyl)-3-oxo-2,3-dihydroisoxazol-4-yl)propanoic acid
2-Amino-3-(5-(tert-butyl)-3-oxo-2,3-dihydroisoxazol-4-yl)propanoicacid
2-AMINO-3-(5-TERT-BUTYL-3-HYDROXY-1,2-OXAZOL-4-YL)PROPANOIC ACID