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Brivaracetam

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Identification
Molecular formula
C11H20N2O2
CAS number
357336-20-0
IUPAC name
ethyl N-[2-[2-[(4-aminobutylamino)carbamoyl]pyrrolidin-1-yl]-1-benzyl-2-oxo-ethyl]carbamate
State
State

Brivaracetam is typically found in a solid state at room temperature. It is stable under normal temperatures and pressures in the laboratory or in controlled environments.

Melting point (Celsius)
88.00
Melting point (Kelvin)
361.15
Boiling point (Celsius)
443.00
Boiling point (Kelvin)
716.15
General information
Molecular weight
270.32g/mol
Molar mass
270.3220g/mol
Density
1.2000g/cm3
Appearence

Brivaracetam has a white to off-white crystalline appearance. It is presented in various pharmaceutical forms, such as tablets and solutions. The solid form is usually in powder or crystalline form, which is often odorless and tasteless.

Comment on solubility

Solubility of Ethyl N-[2-[2-[(4-aminobutylamino)carbamoyl]pyrrolidin-1-yl]-1-benzyl-2-oxo-ethyl]carbamate

The solubility of ethyl N-[2-[2-[(4-aminobutylamino)carbamoyl]pyrrolidin-1-yl]-1-benzyl-2-oxo-ethyl]carbamate (C11H20N2O2) can be influenced by several factors that play a critical role in its interaction with solvents:

  • Polarity: The presence of multiple polar functional groups such as carbamate and amino groups suggests that this compound may exhibit reasonable solubility in polar solvents, including water and alcohols.
  • Hydrogen Bonding: Capable of forming hydrogen bonds, the compound's solubility may significantly increase in protic solvents. The donor and acceptor sites from the -NH and -C=O moieties can engage in interactions with solvent molecules.
  • Hydrophobic Character: The benzyl and pyrrolidine portions contribute to hydrophobicity, which could limit solubility in purely polar solvents. This dual characteristic may lead to nuanced solubility behavior.
  • Temperature Effects: Generally, solubility can vary with temperature; thus, elevated temperatures might enhance solubilization and dissolution rates.

In summary, while the detailed solubility characteristics of ethyl N-[2-[2-[(4-aminobutylamino)carbamoyl]pyrrolidin-1-yl]-1-benzyl-2-oxo-ethyl]carbamate require empirical testing for precise determinations, it is reasonable to anticipate moderate solubility in aqueous and organic solvents due to its unique chemical structure.

Interesting facts

Interesting Facts about Ethyl N-[2-[2-[(4-aminobutylamino)carbamoyl]pyrrolidin-1-yl]-1-benzyl-2-oxo-ethyl]carbamate

Ethyl N-[2-[2-[(4-aminobutylamino)carbamoyl]pyrrolidin-1-yl]-1-benzyl-2-oxo-ethyl]carbamate is a fascinating compound with significant implications in both medicinal chemistry and pharmaceutical development. Here are some key aspects that highlight its importance:

  • Chemical Structure: This compound features a unique arrangement of functional groups which includes amine, carbamate, and pyrrolidine moieties. This diversity allows for various interactions with biological targets.
  • Potential Therapeutic Uses: Compounds with similar structures are often investigated for their potential as antidepressants and anxiolytics. This is due to their ability to modulate neurotransmitter systems in the brain.
  • Biocompatibility: The presence of amino groups generally enhances biocompatibility, making this compound a candidate for research into drug delivery systems or biosensors.
  • Mechanism of Action: The mechanisms through which such compounds operate might involve inhibition of specific enzymes or receptors, leading to potential clinical benefits.
  • Research and Development: Due to its complex structure, the synthesis of this compound can provide an exciting challenge for chemists, often fostering the development of new synthetic techniques.

As researchers delve into the properties and reactions of ethyl N-[2-[2-[(4-aminobutylamino)carbamoyl]pyrrolidin-1-yl]-1-benzyl-2-oxo-ethyl]carbamate, they increasingly uncover its potential to contribute to groundbreaking therapies, enhancing our understanding of chemical interactions within biological systems. Its synthesis, characterization, and application open avenues for innovative approaches in the realm of pharmaceuticals.

Synonyms
SCHEMBL8150669
PD037884