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Ibotenic acid

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Identification
Molecular formula
C5H6N2O4
CAS number
2552-55-8
IUPAC name
2-amino-2-(3-oxoisoxazol-5-yl)acetic acid
State
State

State: At room temperature, ibotenic acid is a solid. It is generally stable under normal conditions but should be handled carefully to prevent exposure or contact.

Melting point (Celsius)
134.00
Melting point (Kelvin)
407.15
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
158.11g/mol
Molar mass
158.1100g/mol
Density
1.7233g/cm3
Appearence

Appearance: Ibotenic acid appears as a white solid. It is typically found in crystalline form, highlighting its purity and distinct chemical structure.

Comment on solubility

Solubility of 2-amino-2-(3-oxoisoxazol-5-yl)acetic acid

2-amino-2-(3-oxoisoxazol-5-yl)acetic acid, with the chemical formula C5H6N2O4, exhibits intriguing solubility characteristics that are worth exploring:

  • Highly Soluble in Water: This compound is anticipated to have good solubility in water, primarily due to its polar functional groups.
  • Influence of Hydrogen Bonds: The presence of amino (-NH2) and carboxylic acid (-COOH) groups facilitates hydrogen bonding, enhancing its interaction with water molecules.
  • Varied Solubility in Organic Solvents: The solubility of this compound in organic solvents can vary, with lower solubility in non-polar solvents due to the polar nature of its functional groups.

Moreover, understanding the solubility behavior of 2-amino-2-(3-oxoisoxazol-5-yl)acetic acid is crucial for its applications in pharmaceuticals and biochemical research, where the solubility can directly impact the compound's efficacy and bioavailability. As a key takeaway, the potency of this compound is significantly influenced by its solubility properties.

Interesting facts

Interesting Facts about 2-amino-2-(3-oxoisoxazol-5-yl)acetic acid

2-amino-2-(3-oxoisoxazol-5-yl)acetic acid is a fascinating compound that belongs to the class of isoxazole derivatives. Here are some noteworthy insights about this intriguing chemical:

  • Biological Significance: This compound is of particular interest in medicinal chemistry due to its potential pharmacological properties. Isoxazole derivatives often exhibit various biological activities, including anti-inflammatory and antimicrobial effects.
  • Structure and Function: The unique structure of 2-amino-2-(3-oxoisoxazol-5-yl)acetic acid combines both the amino acid and isoxazole functional groups. This combination can lead to interesting interactions at the molecular level, influencing how the compound behaves biologically.
  • Applications in Research: Researchers have delved into the applications of isoxazole compounds in developing new drugs. The presence of the isoxazole ring often correlates with enhanced activity against specific biological targets.
  • Synergistic Effects: Compounds like this one are frequently explored for their synergistic effects when combined with other active pharmaceutical ingredients (APIs), paving the way for the design of multi-target therapeutics.
  • Potential in Agriculture: Some studies suggest that isoxazole derivatives may also have applications in agriculture, particularly as agrochemicals that protect crops from pests and pathogens.

In summary, 2-amino-2-(3-oxoisoxazol-5-yl)acetic acid is more than just a chemical compound; it embodies the intersection of chemistry and biology, leading to potential advancements in both medicinal and agricultural fields. As we continue to explore and understand its properties, it may unlock new opportunities for scientific research and innovation.

Synonyms
Ibotenic acid
2552-55-8
Ibotenate
(+/-)-Ibotenic acid
2-amino-2-(3-oxo-2,3-dihydroisoxazol-5-yl)acetic acid
DL-Ibotenic acid
(RS)-Ibotenic acid
44AS82FRSI
alpha-Amino-2,3-dihydro-3-oxo-5-isoxazoleacetic acid
alpha-Amino-3-hydroxy-5-isoxazoleacetic acid
MFCD00069294
NSC 204850
2-amino-2-(3-oxo-1,2-oxazol-5-yl)acetic acid
5-Isoxazoleacetic acid, alpha-amino-2,3-dihydro-3-oxo-
NSC204850
NSC-204850
IBOTENIC ACID [MI]
C5H6N2O4
CHEBI:5854
CHEMBL284895
IBOTENIC ACID [WHO-DD]
DTXSID40893771
IBOTENIC ACID, (+/-)-
4-Isoxazoline-5-acetic acid, alpha-amino-3-oxo-
(RS)-Ibotenic acid;DL-Ibotenic acid
5-Isoxazoleacetic acid, .alpha.-amino-2,3-dihydro-3-oxo-
2-amino-2-(3-oxoisoxazol-5-yl)acetic acid
5-Isoxazoleacetic acid,a-amino-2,3-dihydro-3-oxo-
Acid, Ibotenic
5-Isoxazoleaceticacid,-alpha--amino-2,3-dihydro-3-oxo-,(-alpha-R)-(9CI)
SR-01000075462
UNII-44AS82FRSI
(y)-Ibotenic acid
(?)-Ibotenic acid
(alpha)-Ibotenic acid
alpha-amino-(3-hydroxy-5-isoxazolyl)acetic acid
Lopac0_000651
MLS002153141
SCHEMBL153359
4-Isoxazoline-5-acetic acid, .alpha.-amino-3-oxo-
Ibotenic acid, ~95%, solid
GTPL1371
5-Isoxazoleaceticacid,-alpha--amino-2,3-dihydro-3-oxo-,(-alpha-S)-(9CI)
BDBM82355
IRJCBFDCFXCWGO-UHFFFAOYSA-N
DTXCID701323806
HMS2230A08
HMS3262C03
HMS3266E19
HMS3369N13
HMS3414F03
HMS3678F03
BCP23586
HY-N2311
NSC_1233
Tox21_500651
HB0330
PDSP1_001426
PDSP2_001410
AKOS006228673
AKOS027320609
CCG-204738
FI41653
LP00651
SDCCGSBI-0050631.P002
( inverted question mark)-Ibotenic acid
NCGC00015555-03
NCGC00015555-04
NCGC00015555-05
NCGC00015555-06
NCGC00024524-02
NCGC00024524-03
NCGC00024524-04
NCGC00261336-01
5-Isoxazoleacetic acid,3-dihydro-3-oxo-
a-Amino-3-hydroxy-5-isoxazoleacetic acid
CS-13243
DA-54220
SMR001230640
CAS_2552-55-8
a-Amino-(3-hydroxy-5-isoxazolyl)acetic acid
CS-0020472
EU-0100651
NS00075437
I 2765
L000672
Q411094
SR-01000075462-1
SR-01000075462-3
5-Isoxazoleacetic acid, ?-amino-2,3-dihydro-3-oxo-
BRD-A04628621-001-02-6
2-amino-2-(3-oxo-2,3-dihydroisoxazol-5-yl)aceticacid
4-Isoxazoline-5-acetic acid, alpha-amino-3-oxo-(8ci)
(2S)-2-amino-2-(3-hydroxy-1,2-oxazol-5-yl)acetic acid
Amino-(3-hydroxy-isoxazol-5-yl)-acetic acid(Ibotenic acid)
acetic acid, 2-amino-2-(2,3-dihydro-3-oxo-5-isoxazolyl)-
( inverted question mark)-alpha-Amino-3-hydroxy-5-isoxazoleacetic acid
637-415-7