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2-Bromoheptanoic acid

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Identification
Molecular formula
C7H13BrO2
CAS number
616-05-7
IUPAC name
2-bromoheptanoic acid
State
State

At room temperature, 2-Bromoheptanoic acid is a solid.

Melting point (Celsius)
35.00
Melting point (Kelvin)
308.15
Boiling point (Celsius)
290.00
Boiling point (Kelvin)
563.15
General information
Molecular weight
211.08g/mol
Molar mass
211.0730g/mol
Density
1.4600g/cm3
Appearence

2-Bromoheptanoic acid appears as a light-colored or white crystalline solid. This compound may also present a somewhat waxy texture at room temperature.

Comment on solubility

Solubility of 2-Bromoheptanoic Acid

2-bromoheptanoic acid, with the chemical formula C7H13BrO2, demonstrates intriguing solubility characteristics that can be explored through various factors:

  • Polarity: The presence of the carboxylic acid group (-COOH) significantly influences its solubility. Carboxylic acids are generally polar and have the ability to engage in hydrogen bonding with water molecules.
  • Hydrophobic Chain: The bromoheptanoic acid features a long carbon chain which is hydrophobic in nature. This characteristic can limit its solubility in polar solvents.
  • Solvent Dependence: 2-bromoheptanoic acid is likely to be more soluble in organic solvents, such as alcohols and ethers, compared to water.

Overall, the solubility of 2-bromoheptanoic acid can be summarized as:

  1. More soluble in polar solvents due to the presence of the carboxylic group.
  2. Less soluble in water due to the hydrophobic carbon chain component.
  3. Variable solubility in non-polar solvents influenced by its overall structure.

Understanding the solubility properties of 2-bromoheptanoic acid is essential in various chemical applications, particularly in contexts where dissolution and reactivity are pivotal.

Interesting facts

Interesting Facts About 2-Bromoheptanoic Acid

2-Bromoheptanoic acid is a fascinating compound within the realm of organic chemistry, and its unique structure and reactivity make it a subject of study for various applications. Here are some engaging insights:

  • Structural Features: This compound contains a bromo group attached to the second carbon of heptanoic acid, providing it with distinctive reactivity. The presence of the bromine atom introduces a site for nucleophilic substitution reactions, making it particularly useful in organic synthesis.
  • Synthesis Potential: 2-Bromoheptanoic acid can be synthesized through various methods, often utilizing bromoalkane reactions. This allows chemists to explore various pathways to create even more complex molecules, further expanding its applicability.
  • Biological Significance: Compounds like 2-bromoheptanoic acid play a role in biochemical research. By modifying fatty acid chains, they can be used to study lipid metabolism and the effects of acyl chain length on biological properties.
  • Versatile Derivatives: The reactions involving 2-bromoheptanoic acid can yield a plethora of derivatives that are useful in pharmaceuticals, agrochemicals, and materials science. The derivative products can exhibit unique biological activities and can be tailored for specific functions.
  • Educational Value: For chemistry students, 2-bromoheptanoic acid serves as an excellent model compound to explore various concepts, including substitution reactions, stereochemistry, and functional group transformations.

As noted by chemists, "The exploration of derivatives from simple compounds often leads to remarkable discoveries." This emphasizes the importance of 2-bromoheptanoic acid in the interconnected web of chemical research and development.

In conclusion, the study of 2-bromoheptanoic acid not only enhances our understanding of organic compounds but also paves the way for innovative approaches in synthetic chemistry and medicinal applications.

Synonyms
2-BROMOHEPTANOIC ACID
2624-01-3
A-BROMOHEPTANOIC ACID
2-bromo-heptanoic acid
Heptanoic acid, 2-bromo-
EINECS 220-087-0
A-BROMOHEPTANOICACID
SCHEMBL1036505
NQRFAUVGDLHPGH-UHFFFAOYSA-
DTXSID60949103
DB-046907
NS00048737
InChI=1/C7H13BrO2/c1-2-3-4-5-6(8)7(9)10/h6H,2-5H2,1H3,(H,9,10)