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Tribenzyl borate

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Identification
Molecular formula
C21H21BO3
CAS number
1660-88-8
IUPAC name
tribenzyl borate
State
State

At room temperature, tribenzyl borate is in a liquid state. It remains stable under normal conditions but is sensitive to moisture.

Melting point (Celsius)
-37.00
Melting point (Kelvin)
236.15
Boiling point (Celsius)
324.00
Boiling point (Kelvin)
597.15
General information
Molecular weight
308.26g/mol
Molar mass
308.2570g/mol
Density
1.1320g/cm3
Appearence
Tribenzyl borate typically appears as a colorless to pale yellow liquid. It has a characteristic aromatic smell due to its benzyl group components.
Comment on solubility

Solubility of Tribenzyl Borate

Tribenzyl borate, with the chemical formula C21H21B1O3, exhibits interesting solubility characteristics that are noteworthy.

Key points regarding the solubility of tribenzyl borate:

  • Solvent Compatibility: This compound is generally soluble in organic solvents such as benzene, ethanol, and chloroform.
  • Water Solubility: Tribenzyl borate has very limited solubility in water, making it more suitable for organic phase reactions.
  • Temperature Dependence: As with many organic compounds, its solubility can vary significantly with temperature; higher temperatures often enhance solubility.

When discussing such solubility levels, it can be said that tribenzyl borate behaves predominantly as a non-polar compound due to the presence of benzyl groups, which can significantly influence its interaction with solvents. Therefore, for effective applications, particularly in synthetic chemistry, one must consider these solubility behaviors to ensure successful chemical reactions and formulations.


Interesting facts

Interesting Facts About Tribenzyl Borate

Tribenzyl borate, a fascinating organoborane compound, is known for its diverse applications and intriguing chemical properties. Here are some key points to consider:

  • Versatile Applications: This compound is widely utilized in the chemical industry, particularly in the synthesis of other organic compounds and as a reagent in various chemical reactions.
  • Unique Structure: The presence of three benzyl groups attached to a central boron atom contributes to its distinctive properties. This structure makes it a valuable intermediate in organic synthesis.
  • Ligand Behavior: Tribenzyl borate acts as a soft Lewis acid, making it a useful ligand in coordination chemistry. It can form complexes with various metals, enhancing the reactivity and utility of those metals.
  • Environmental Considerations: Understanding tribenzyl borate's behavior in the environment is important. Its properties can influence the degradation and bioavailability of boron in ecological systems.
  • Research Potential: Scientists are continually exploring the potential of this compound in fields like catalysis, pharmaceuticals, and materials science, showcasing its significance in modern chemistry.

In summary, tribenzyl borate is more than just a compound; it's a gateway to fascinating chemical reactions and applications that highlight the importance of organoboron chemistry in various scientific fields. As one researcher noted, "Understanding boron compounds like tribenzyl borate can open new pathways in organic synthesis, revealing potential that is just waiting to be discovered."

Synonyms
Tribenzyl borate
Boric acid (H3BO3), tris(phenylmethyl) ester
654-433-0
2467-18-7
BORIC ACID, TRIBENZYL ESTER
tribenzylborate
NSC 164000
BRN 1997372
AI3-60046
boric acid tribenzyl ester
SCHEMBL51017
4-06-00-02589 (Beilstein Handbook Reference)
DTXSID40179406
IJJNTMLAAKKCML-UHFFFAOYSA-N
NSC164000
AKOS024323137
NSC-164000
Boric acid(h3bo3),tris(phenylmethyl)ester