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5-Fluoropentyl benzoate

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Identification
Molecular formula
C12H15FO2
CAS number
1239457-73-3
IUPAC name
5-fluoropentyl benzoate
State
State

At room temperature, 5-Fluoropentyl benzoate is a liquid.

Melting point (Celsius)
-18.00
Melting point (Kelvin)
255.15
Boiling point (Celsius)
315.00
Boiling point (Kelvin)
588.15
General information
Molecular weight
210.25g/mol
Molar mass
210.2290g/mol
Density
1.0802g/cm3
Appearence

5-Fluoropentyl benzoate typically appears as a colorless to pale yellow liquid. It is clear in clarity without any particulate matter.

Comment on solubility

Solubility of 5-fluoropentyl benzoate

5-fluoropentyl benzoate, with its unique structure, presents interesting solubility characteristics. This compound's solubility is influenced by its molecular interactions and structure. Here are some important points regarding its solubility:

  • Polar vs. Nonpolar Solvents: 5-fluoropentyl benzoate is expected to be more soluble in nonpolar solvents due to its alkyl chain, which is hydrophobic in nature. However, the presence of the fluorine atom can introduce some polarity.
  • Temperature Effects: Like many organic compounds, the solubility of 5-fluoropentyl benzoate typically increases with temperature. This phenomenon can enhance its dissolution rates in certain solvents.
  • Concentration Stability: It may exhibit significant solubility at higher concentrations, leading to interesting applications in various chemical processes.
  • Solubility Limitations: While soluble in many organic solvents, it might face limitations in aqueous environments owing to its overall hydrophobic character.

In conclusion, the solubility of 5-fluoropentyl benzoate is a balance of its hydrophobic alkyl chain and the influence of its functional groups. Understanding these interactions is essential for applications in organic synthesis and material science.

Interesting facts

Interesting Facts About 5-Fluoropentyl Benzoate

5-Fluoropentyl benzoate is a fascinating compound that belongs to the class of benzoates, which are esters derived from benzoic acid. This particular compound chemically combines a fluorinated chain with a benzoate group, leading to intriguing properties and applications.

Key Features

  • Fluorine Substitution: The presence of a fluorine atom significantly alters the physical and chemical properties of organic compounds. Fluorine is highly electronegative and introduces unique attributes such as increased stability and lipophilicity.
  • Applications in Research: Compounds like 5-fluoropentyl benzoate are often studied for their potential use in pharmaceuticals, particularly in the development of novel therapeutic agents.
  • Biological Activity: Some studies suggest that benzoate derivatives can exhibit various biological activities, potentially making 5-fluoropentyl benzoate a candidate for further investigation in drug design.

Operational Insights

When it comes to synthesis, compounds like 5-fluoropentyl benzoate are typically produced through esterification reactions, where an alcohol reacts with a carboxylic acid in the presence of an acid catalyst. This process might involve:

  1. Reacting 5-fluoropentanol with benzoic acid.
  2. Utilizing reagents such as sulfuric acid as a catalyst to facilitate the reaction.

Final Thoughts

As a student of chemistry or a seasoned scientist, exploring compounds like 5-fluoropentyl benzoate can provide valuable insights into the intricate world of organic synthesis and its implications in various fields. The blend of fluorine and benzoate may reveal opportunities for interdisciplinary research, bridging organic chemistry with pharmacology.

Synonyms
583-16-4
5-Fluoroamyl benzoate
BENZOIC ACID, 5-FLUOROPENTYL ESTER
5-Fluoropentyl ester of benzoic acid
BRN 3265567
DTXSID10207023
4-09-00-00292 (Beilstein Handbook Reference)
DTXCID10129514
Benzoic Acid 5-Fluoropentyl Ester