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Nonylboronic acid

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Identification
Molecular formula
C9H21BO2
CAS number
4741-86-4
IUPAC name
nonylboronic acid
State
State

At room temperature, Nonylboronic acid is a liquid, which can be described as oily due to its viscous nature.

Melting point (Celsius)
-60.00
Melting point (Kelvin)
213.15
Boiling point (Celsius)
300.00
Boiling point (Kelvin)
573.15
General information
Molecular weight
186.08g/mol
Molar mass
186.1700g/mol
Density
0.9395g/cm3
Appearence

Nonylboronic acid appears as a colorless to pale yellow liquid under normal conditions. It may also be if refrigerated or exposed to lower temperatures. The compound usually has an oily texture due to its organic nature with a medium-length carbon chain.

Comment on solubility

Solubility of Nonylboronic Acid

Nonylboronic acid, with the chemical formula C9H13BO2, exhibits some interesting solubility characteristics that warrant attention:

  • Polarity: The presence of the boronic acid group confers a degree of polarity to this compound, influencing its interaction with solvents.
  • Solvent Compatibility: Nonylboronic acid is generally soluble in polar organic solvents such as methanol and ethanol. However, it displays limited solubility in nonpolar solvents like hexane.
  • Water Solubility: This compound has low water solubility due to its hydrophobic nonyl group, but may show some degree of solubility in water under specific conditions (e.g., with variations in pH).
  • Concentration Effects: As the concentration of nonylboronic acid increases, solubility can be impacted, potentially leading to precipitation in less polar environments.

In summary, the solubility of nonylboronic acid is heavily influenced by its structural attributes, solvent type, and environmental conditions. Understanding these factors is crucial for its effective application in chemical processes.

Interesting facts

Interesting Facts About Nonylboronic Acid

Nonylboronic acid, known for its unique structural characteristics, is a fascinating compound in the realm of organoboron chemistry. Here are some intriguing facts about this compound:

  • Applications in Organic Synthesis: Nonylboronic acid is primarily utilized as a versatile building block in organic synthesis, especially in the preparation of complex organic molecules.
  • Reactivity: Due to the presence of the boronic acid group, nonylboronic acid exhibits distinct reactivity patterns, including cross-coupling reactions with organic halides. This property allows chemists to forge new carbon-carbon bonds effectively.
  • Biological Applications: Beyond its utility in synthetic chemistry, nonylboronic acid has been researched for its potential applications in biological systems, particularly in drug delivery and targeting.
  • Environmental Considerations: As with many organoboron compounds, it’s essential to consider the environmental implications and toxicity associated with nonylboronic acid, leading to ongoing research for safer alternatives.
  • Interesting Structure: The branched structure of nonylboronic acid provides unique properties compared to linear boronic acids, making it a topic of interest for materials science and polymer chemistry.

The exploration of nonylboronic acid continues to reveal its potential, both in laboratory settings and industrial applications. As researchers delve deeper, they may uncover even more capabilities for this intriguing compound.

Synonyms
NONYLBORONIC ACID
3088-78-6
1-Nonaneboronic acid
Boronic acid, B-nonyl-
Boronic acid, nonyl-
BRN 1741032
WLN: QBQ9
SCHEMBL6917203
RHPOAOZKVCLNPE-UHFFFAOYSA-
DTXSID20184891
NSC53325
NSC 53325
NSC-53325
AKOS013013909
InChI=1/C9H21BO2/c1-2-3-4-5-6-7-8-9-10(11)12/h11-12H,2-9H2,1H3