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Phenylalanine methyl ester hydrobromide

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Identification
Molecular formula
C9H11BrNO2
CAS number
3184-77-0
IUPAC name
(2-amino-2-oxo-1-phenyl-ethyl)ammonium;bromide
State
State

At room temperature, the compound is in a solid state, typically existing as a crystalline powder that is stable under standard conditions.

Melting point (Celsius)
252.00
Melting point (Kelvin)
525.15
Boiling point (Celsius)
210.00
Boiling point (Kelvin)
483.15
General information
Molecular weight
246.10g/mol
Molar mass
246.1020g/mol
Density
1.6000g/cm3
Appearence

The compound typically appears as a white to off-white crystalline powder. It is often characterized by its crystalline solid form, which is common among many ammonium bromide salts.

Comment on solubility

Solubility of (2-amino-2-oxo-1-phenyl-ethyl)ammonium bromide

The compound (2-amino-2-oxo-1-phenyl-ethyl)ammonium bromide, often abbreviated as this complex name, showcases particular solubility characteristics that are noteworthy:

  • Ammonium Salts: Compounds containing ammonium ions generally exhibit high solubility in water. As an ammonium salt, this bromide likely follows that trend.
  • Polarity: The presence of polar functional groups, such as the amino and carbonyl groups, contributes to its overall solubility in polar solvents like water.
  • Bromide Ion Influence: Bromide ions (Br-) are known to form strong hydrogen bonds with water molecules, enhancing the solubility of this compound in aqueous environments.

In conclusion, you can expect that (2-amino-2-oxo-1-phenyl-ethyl)ammonium bromide would be readily soluble in polar solvents, particularly water, due to its ionic nature, the influence of its constituent functional groups, and the behavior of the bromide ion. This solubility profile plays a critical role in its applications in various chemical reactions and processes.

Interesting facts

Interesting Facts about (2-amino-2-oxo-1-phenyl-ethyl)ammonium Bromide

(2-amino-2-oxo-1-phenyl-ethyl)ammonium bromide is a fascinating compound that showcases the intricate relationships between structure and function in chemical compounds. This compound falls under the category of quaternary ammonium salts, which are often utilized in various applications due to their unique properties. Here are some intriguing aspects of this compound:

  • Biological Importance: Compounds like this one often exhibit significant biological activity, making them crucial in pharmaceutical research. They are of interest for developing new drugs, particularly in areas like antimicrobial and anti-inflammatory therapies.

  • Chemical Reactivity: The presence of the amino and carbonyl groups in the structure provides various opportunities for chemical reactivity. These functional groups are known to be involved in important biochemical processes, such as enzyme catalysis and ligand formation.

  • Versatile Applications: Quaternary ammonium compounds are widely used as surfactants, antiseptics, and stabilizers in different industrial processes. This compound could potentially serve similar roles, contributing to advancements in material sciences or biotechnology.

  • Structure-Activity Relationship: Studying compounds like (2-amino-2-oxo-1-phenyl-ethyl)ammonium bromide can enhance our understanding of structure-activity relationships (SAR) in medicinal chemistry, guiding the design of more effective drugs with fewer side effects.

This compound is an excellent example of how subatomic structures can lead to large-scale implications in various fields of science, from medicinal chemistry to materials science. With ongoing research, there is a great potential for discovering new properties and applications for (2-amino-2-oxo-1-phenyl-ethyl)ammonium bromide, paving the way for advancements that could benefit society as a whole.

Synonyms
2-Amino-2-phenylacetamide hydrobromide
3263-99-8
alpha-Amino-alpha-phenylacetamid hydrobromid [German]
ACETAMIDE, 2-AMINO-2-PHENYL-, HYDROBROMIDE
alpha-Amino-alpha-phenylacetamid hydrobromid