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2-Benzyl-3-iodopropanoic acid

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Identification
Molecular formula
C10H11IO2
CAS number
.
IUPAC name
2-benzyl-3-iodo-propanoic acid
State
State

At room temperature, 2-benzyl-3-iodopropanoic acid is in a solid state. It has a crystalline structure that is consistent with its molecular arrangement. The compound is generally stable in this state but should be stored in a cool, dry place to prevent decomposition or absorption of moisture.

Melting point (Celsius)
110.00
Melting point (Kelvin)
383.15
Boiling point (Celsius)
318.00
Boiling point (Kelvin)
591.15
General information
Molecular weight
298.08g/mol
Molar mass
298.0840g/mol
Density
1.5540g/cm3
Appearence

2-Benzyl-3-iodopropanoic acid is typically a solid compound. It may appear as a crystalline powder or granules that are off-white to pale yellow in color. Moisture and exposure to air can potentially cause discoloration, altering its appearance, which should be handled under controlled conditions to maintain its stability and color.

Comment on solubility

Solubility of 2-benzyl-3-iodo-propanoic acid (C10H11IO2)

2-benzyl-3-iodo-propanoic acid, an organic compound featuring both an aromatic ring and a functional carboxylic acid group, presents interesting solubility characteristics. Its solubility can be influenced by various factors:

  • Polarity: The presence of the carboxylic acid functional group means that this compound has polar characteristics, which can facilitate solubility in polar solvents such as water.
  • Hydrophobic Interactions: The aromatic benzyl group contributes to hydrophobicity, which may limit solubility in aqueous environments. This can create a balance in how well the compound dissolves.
  • Temperature: As with many organic acids, solubility may increase with temperature, promoting dissolution in higher energy environments.
  • pH Levels: The acidity of the environment will also influence solubility, as lower pH levels can lead to ionization of the carboxylic group, enhancing solubility in water.

In summary, the solubility of 2-benzyl-3-iodo-propanoic acid is characterized by a delicate interplay of polar and non-polar interactions, making it more soluble in suitable solvents tailored to its unique chemical structure. Understanding this solubility profile is crucial in various applications, from synthesis to formulation.

Interesting facts

Interesting Facts about 2-benzyl-3-iodo-propanoic acid

2-benzyl-3-iodo-propanoic acid is a fascinating compound that showcases the interesting interplay between organic chemistry and medicinal applications. Here are some intriguing aspects of this compound:

  • Structural Significance: The molecular structure of 2-benzyl-3-iodo-propanoic acid highlights the importance of iodine substitution in organic molecules, which can dramatically affect their reactivity and properties. The presence of the aromatic benzyl group also contributes to the stability and electronic characteristics of the compound.
  • Role in Synthesis: This compound serves as an important intermediate in various synthetic pathways. It is often used in the preparation of more complex organic molecules, particularly in pharmaceutical development.
  • Medicinal Chemistry: Due to its unique chemical structure, 2-benzyl-3-iodo-propanoic acid has been studied for potential biological activities. Compounds containing similar structures may exhibit anti-inflammatory, analgesic, or other therapeutic properties, making them attractive targets for drug discovery.
  • Reactivity: The iodine atom in the compound can undergo various chemical reactions, such as nucleophilic substitution and electrophilic addition, common reactions in the realm of organic synthesis. Such reactivity plays a pivotal role in its application in diverse chemical transformations.
  • Synthetic Routes: The compound can be synthesized through different methods, including the introduction of the iodo group via electrophilic aromatic substitution or by using iodinated precursors, providing chemists with multiple strategies for its synthesis.

In summary, 2-benzyl-3-iodo-propanoic acid is more than just a chemical compound; it represents the synergy between structural chemistry and an array of applications in pharmaceuticals. Its properties and potential uses highlight the thrilling world of organic synthesis and chemical reactions.

Synonyms
SCHEMBL4309170
PD041490