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N-(4-bromophenyl)aspartic acid

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Identification
Molecular formula
C9H8BrNO4
CAS number
15014-85-8
IUPAC name
2-(4-bromoanilino)propanedioic acid
State
State

At room temperature, N-(4-bromophenyl)aspartic acid is typically found in a solid state. It forms as a crystalline solid that can be easily handled at ambient conditions.

Melting point (Celsius)
204.00
Melting point (Kelvin)
477.20
Boiling point (Celsius)
591.00
Boiling point (Kelvin)
864.00
General information
Molecular weight
274.06g/mol
Molar mass
274.0640g/mol
Density
2.2000g/cm3
Appearence

The compound typically appears as a crystalline solid. The color can range from white to a slightly off-white hue, indicating purity and potential presence of impurities.

Comment on solubility

Solubility of 2-(4-bromoanilino)propanedioic acid (C9H8BrNO4)

The solubility of 2-(4-bromoanilino)propanedioic acid can be quite intriguing due to its specific functional groups and structure. Generally, the solubility of a compound like this will be influenced by several factors:

  • Polarity: The presence of the carboxylic acid groups makes this compound polar, which tends to enhance solubility in polar solvents like water.
  • Hydrogen Bonding: The ability to form hydrogen bonds with water can significantly increase solubility. Since this compound contains acidic groups, it can engage in hydrogen bonding.
  • Electrostatic Interactions: The bromine substituent may also introduce additional considerations regarding solubility, as its electronegativity can affect the compound's net polarity.

Despite these favorable solubility factors, it is essential to remember that:

  • Solubility in water may still be limited due to the hydrophobic nature of the aromatic ring.
  • In nonpolar solvents, the solubility might be significantly reduced because of the compound's polar groups.

In conclusion, while 2-(4-bromoanilino)propanedioic acid displays potential for solubility in polar solvents owing to its functional groups, practical solubility can vary, leading to a complex behavior in real-world applications. As always, conducting experimental solubility tests remains crucial.

Interesting facts

Interesting Facts about 2-(4-bromoanilino)propanedioic acid

2-(4-bromoanilino)propanedioic acid is a fascinating compound that holds significance in both organic chemistry and various industrial applications. This compound is notable for its unique structural features and potential roles in the field of medicinal chemistry.

Key Features

  • Bromine Presence: The inclusion of a bromine atom in the structure can enhance the compound's reactivity and introduces interesting properties that may be harnessed in chemical synthesis.
  • Potential Biological Activity: Due to its anilino group, the compound may exhibit biological activities that could be valuable for developing pharmaceuticals, specifically in targeting certain diseases.
  • Acidic Nature: The presence of carboxylic acid functional groups in the structure may lead to interesting interactions with other compounds, making it useful in drug design.

Applications in Chemistry

This compound serves as a building block in organic synthesis and can be utilized in various reactions to produce more complex molecules. It’s essential in the synthesis of novel materials and can contribute to the development of therapeutics and agrochemicals.

A Fascinating Quote

As chemists often say, “The most beautiful thing we can experience is the mysterious—it is the source of all true art and science.” 2-(4-bromoanilino)propanedioic acid embodies this mystery, inviting exploration within the realms of its chemistry and potential applications.

Overall, this compound exemplifies the complexity and beauty of chemical structures, indicating how a single modification, such as bromination, can lead to profound implications in science and industry.

Synonyms
SCHEMBL7823472
AKOS024331677
2-(4-BROMO-PHENYLAMINO)-MALONIC ACID