Skip to main content

Piracetam

ADVERTISEMENT
Identification
Molecular formula
C6H10N2O2
CAS number
7491-74-9
IUPAC name
2-(4-hydroxy-2-oxo-pyrrolidin-1-yl)acetamide
State
State

At room temperature, Piracetam is a solid, typically appearing as a white crystalline powder.

Melting point (Celsius)
151.00
Melting point (Kelvin)
424.15
Boiling point (Celsius)
452.00
Boiling point (Kelvin)
725.15
General information
Molecular weight
142.16g/mol
Molar mass
142.1560g/mol
Density
1.3500g/cm3
Appearence

Piracetam typically appears as a white crystalline powder that is soluble in water and alcohol, and it may have a slightly characteristic odor. It has no color in its pure solid state.

Comment on solubility

Solubility of 2-(4-hydroxy-2-oxo-pyrrolidin-1-yl)acetamide

The compound 2-(4-hydroxy-2-oxo-pyrrolidin-1-yl)acetamide, with the chemical formula C6H10N2O2, exhibits intriguing solubility characteristics due to its structural features. Understanding its solubility can be crucial for applications in various chemical and biological systems.

Solubility Characteristics

  • Solvent Interaction: The presence of both hydroxyl group and amide functionalities enhances its interaction with polar solvents.
  • Solubility in Water: This compound is expected to be moderately soluble in water due to hydrogen bonding capabilities.
  • Other Solvents: It may also show varying solubility in organic solvents like ethanol and dimethyl sulfoxide (DMSO), which can be attributed to its polar nature.

Factors Influencing Solubility

Several factors can influence the solubility of this compound, including:

  • Temperature: Generally, solubility increases with temperature in many solvents.
  • pH: The ionization state of the amide and hydroxyl groups can change depending on the pH, affecting solubility.
  • Concentration: Higher concentrations might lead to saturation, thereby influencing the solubility limit.

In conclusion, the solubility of 2-(4-hydroxy-2-oxo-pyrrolidin-1-yl)acetamide is influenced by its functional groups and the solvent environment. Understanding these relationships is essential for optimization in synthesis and application.

Interesting facts

Interesting Facts about 2-(4-hydroxy-2-oxo-pyrrolidin-1-yl)acetamide

2-(4-hydroxy-2-oxo-pyrrolidin-1-yl)acetamide, often referred to in the scientific community for its unique structure and potential applications, is a compound of significant interest in medicinal chemistry. Here are some engaging insights:

  • Biological Relevance: This compound has garnered attention for its role in various biochemical pathways, particularly in the synthesis of important biomolecules. Its functional groups contribute to its interaction with biological targets.
  • Structure Activity Relationships (SAR): The presence of the pyrrolidinyl moiety enables it to exhibit diverse biological activities, making it a potential candidate for drug development.
  • Potential Therapeutic Applications: Research suggests that this compound may play a role in the development of therapeutic agents for conditions such as neurological disorders or metabolic syndromes, owing to its structural similarities with known bioactive substances.
  • Mechanism of Action: Like many compounds in medicinal chemistry, understanding the molecular interactions of 2-(4-hydroxy-2-oxo-pyrrolidin-1-yl)acetamide with enzymes and receptors is crucial for elucidating its mechanism of action and optimizing its efficacy.
  • Synthetic Pathways: The synthesis of this compound often involves multi-step organic reactions that highlight the intricate nature of modern organic synthesis and the creativity required in designing novel pathways.

As a student or scientist delving into organic chemistry, appreciating compounds like 2-(4-hydroxy-2-oxo-pyrrolidin-1-yl)acetamide can enhance your understanding of the relationship between structure and function, paving the way for innovative approaches in drug design and molecular biology. The beauty of chemistry lies in its ability to unveil the potential locked within molecular frameworks.

Synonyms
oxiracetam
62613-82-5
2-(4-hydroxy-2-oxopyrrolidin-1-yl)acetamide
4-Hydroxy-2-oxopyrrolidine-N-acetamide
1-Pyrrolidineacetamide, 4-hydroxy-2-oxo-
CGP 21690E
4-Hydroxy-2-oxo-1-pyrrolidineacetamide
ISF 2522
(+-)-Oxiracetam
ISF-2522
CGP-21690E
CT-848
Oxiracetam [INN:BAN]
Oxiracetam(Random Configuration)
GNF-PF-1005
Oxiracetam (INN)
DTXSID9045180
UNII-P7U817352G
OXIRACETAM [MI]
OXIRACETAM [INN]
OXIRACETAM [JAN]
(+-)-4-Hydroxy-2-oxo-1-pyrrolidineacetamide
MFCD00242951
Hydroxypiracetam
P7U817352G
OXIRACETAM [MART.]
1-Pyrrolidineacetamide, 4-hydroxy-2-oxo-, (+-)-
OXIRACETAM [WHO-DD]
DTXCID7025180
Neuromet
5-21-12-00019 (Beilstein Handbook Reference)
NCGC00015768-02
Neuractiv
4-HYDROXY-2-OXO-PYRROLIDINACETAMIDE
OXIRACETAM (MART.)
4-Hydroxypiracetam
2-(4-HYDROXY-2-OXO-1-PYRROLIDINYL)ACETAMIDE
Oxiracetamum
Oxiracetamum [INN-Latin]
(R)-(+)-Oxiracetam
CCRIS 4221
BRN 1529719
oxiractam
Oriest
Oxiracetam (Standard)
Lopac0_000933
CHEMBL36633
SCHEMBL526050
HY-B1715R
N06BX07
CHEBI:134788
IHLAQQPQKRMGSS-UHFFFAOYSA-N
HMS3262L08
HMS3652J06
HMS3885B17
BCP06209
BCP31146
HY-B1715
Tox21_110218
Tox21_500933
AC-670
CS3412
s4270
AKOS013252523
AB05478
CCG-205014
CS-8012
DB13601
FO26628
LP00933
SDCCGSBI-0050907.P002
4-hydroxypyrrolidin-2-on-1-yl acetamide
NCGC00015768-03
NCGC00015768-04
NCGC00015768-07
NCGC00094242-01
NCGC00094242-02
NCGC00261618-01
4-hydroxy-2-oxopyrrolidin-1-yl-acetamide
68567-97-5
AS-11801
CAS-62613-82-5
DB-054213
EU-0100933
NS00122220
O0398
SW220157-1
2-(4-hydroxypyrrolidin-2-on-1-yl) acetamide
EN300-75437
D07346
O 3011
Q415099
SR-01000076046
SR-01000076046-1
R-Oxiracetam; (R)-ISF-2522;(R)-(+)-Oxiracetam
Z1178486698
4-Hydroxy-2-oxo-1-pyrrolidineacetamide;Hydroxypiracetam;2-(4-Hydroxy-2-oxopyrrolidin-1-yl)acetamide