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Triphenylmethyl benzoate

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Identification
Molecular formula
C26H22O3
CAS number
79-28-7
IUPAC name
[3-benzoyloxy-2,2-bis(benzoyloxymethyl)propyl] benzoate
State
State

At room temperature, Triphenylmethyl benzoate is in a solid state, typically found as a crystalline powder. This solid state is characteristic for many aromatic ester compounds.

Melting point (Celsius)
120.00
Melting point (Kelvin)
393.15
Boiling point (Celsius)
300.00
Boiling point (Kelvin)
573.15
General information
Molecular weight
362.38g/mol
Molar mass
362.3780g/mol
Density
1.2000g/cm3
Appearence

Triphenylmethyl benzoate typically appears as a white to off-white crystalline powder. It is generally used in academic and industrial settings, and its crystalline form is common for its applications.

Comment on solubility

Solubility of [3-benzoyloxy-2,2-bis(benzoyloxymethyl)propyl] benzoate

The solubility of [3-benzoyloxy-2,2-bis(benzoyloxymethyl)propyl] benzoate is an intriguing topic due to its complex structure and functional groups. This compound, with multiple benzoyloxy and benzoate moieties, exhibits varying solubility characteristics depending on the solvent used.

Factors Influencing Solubility

When evaluating the solubility of this compound, several key factors come into play:

  • Polarity of Solvent: The presence of aromatic rings suggests that the compound may be more soluble in non-polar solvents like toluene or hexane, rather than polar solvents like water.
  • Hydrogen Bonding: The potential for hydrogen bonding through the -O- groups may enhance solubility in polar solvents, but the bulkiness of the molecule could hinder this effect.
  • Temperature Effects: Solubility may increase with temperature, as more energy can allow for better interaction between solute and solvent.

Solubility Observations

In practical terms, [3-benzoyloxy-2,2-bis(benzoyloxymethyl)propyl] benzoate may exhibit:

  • Moderate solubility in organic solvents.
  • Low solubility in water, primarily due to its hydrophobic character.
  • Improved solubility in mixtures of solvents, particularly those that contain aromatic components.

In conclusion, understanding the solubility of [3-benzoyloxy-2,2-bis(benzoyloxymethyl)propyl] benzoate is crucial for its applications in various chemical processes, and its behavior can be finely tuned by adjusting the solvent conditions.

Interesting facts

Interesting Facts about [3-benzoyloxy-2,2-bis(benzoyloxymethyl)propyl] benzoate

[3-benzoyloxy-2,2-bis(benzoyloxymethyl)propyl] benzoate is an intriguing compound that showcases the complexity and beauty of organic chemistry. This compound falls under the category of esters, which are commonly formed from the reaction of acids and alcohols. Here are some interesting points about this compound:

  • Multi-Functional Groups: The presence of multiple benzoyloxy groups in its structure allows for enhanced reactivity and potential applications in various chemical reactions.
  • Applications in Synthesis: Compounds like this one often serve as intermediates in the synthesis of more complex molecules, particularly in the fields of pharmaceuticals and organic materials.
  • Biological Relevance: Due to its structural characteristics, it has potential uses in drug development, where specific functional groups can improve pharmacokinetics and bioavailability.
  • Analytical Techniques: Scientists utilize various analytical methods, such as NMR (Nuclear Magnetic Resonance) and Mass Spectrometry, to study and verify the structure of this compound, ensuring its correct synthesis in the lab.
  • Visualize Reaction Pathways: The study of this compound allows chemists to visualize purely organic reaction pathways and aids in understanding the behavior of esters within organic systems.

As a compound rich in functional diversity, it exemplifies how careful manipulation of molecular architecture can lead to materials with interesting chemical properties. This opens up new avenues for research and development within the field of chemistry.

In the words of renowned chemist Richard Smalley, "Research is to see what everybody has seen and to think what nobody has thought." This statement embodies the spirit of discovering the potential of compounds like [3-benzoyloxy-2,2-bis(benzoyloxymethyl)propyl] benzoate!

Synonyms
Pentaerythritol tetrabenzoate
Pentaerythrityl Tetrabenzoate
Uniplex 552
CCRIS 5971
EINECS 224-079-8
U7L44GIS4O
2,2-Bis((benzoyloxy)methyl)-1,3-propanediol dibenzoate
Pentaerythritol, tetrabenzoate
NSC 166502
BRN 3513249
DTXSID8024608
1,3-Propanediol, 2,2-bis((benzoyloxy)methyl)-, dibenzoate
2,2-Bis((benzoyloxy)methyl)dibenzoate propanediol
NSC-166502
DTXCID804608
1,3-Propanediol, 2,2-bis[(benzoyloxy)methyl]-, dibenzoate
1,3-Propanediol, 2,2-bis((benzoyloxy)methyl)-, 1,3-dibenzoate
2,2-BIS[(BENZOYLOXY)METHYL]-1,3-PROPANEDIOL DIBENZOATE
BIS((BENZOYLOXY)METHYL)-1,3-PROPANEDIOL DIBENZOATE, 2,2-
2,2-Bis[(benzoyloxy)methyl]dibenzoate propanediol
1,3-Propanediol, 2,2-bis[(benzoyloxy)methyl]-, 1,3-dibenzoate
BENZOFLEX S 552
PENTAERYTHRITYL TETRABENZOATE [INCI]
1,3-Propanediol, 2,2-bis(benzoyloxy)methyl-, dibenzoate
2,2-BIS((BENZOYLOXY)METHYL)DIBENZOATE-1,3-PROPANEDIOL
224-079-8
4196-86-5
Benzoflex S-552
[3-benzoyloxy-2,2-bis(benzoyloxymethyl)propyl] benzoate
2,2-bis((benzoyloxy)methyl)propane-1,3-diyl dibenzoate
Benzoic acid, tetraester with pentaerythritol
3-(Benzoyloxy)-2,2-bis[(benzoyloxy)methyl]propyl benzoate
Propanediol (2,2-bis (benzoyloxy)methyl)-dibenzoate
3-[(phenylcarbonyl)oxy]-2,2-bis{[(phenylcarbonyl)oxy]methyl}propyl benzoate
UNII-U7L44GIS4O
MFCD00020676
SCHEMBL27620
CHEMBL1533629
MINJAOUGXYRTEI-UHFFFAOYSA-
Pentaerythritol tetrabenzoate, 96%
Tox21_200988
BBL000680
NSC166502
STK366686
AKOS001606906
NCGC00091832-01
NCGC00091832-02
NCGC00258541-01
VS-00665
CAS-4196-86-5
CS-0156545
NS00021149
P1230
1, 2,2-bis[(benzoyloxy)methyl]-, dibenzoate
SR-01000408140
SR-01000408140-1
Q27290795
[3-(benzoyloxy)-2,2-bis(benzoyloxymethyl)propyl] benzoate
3-(Benzoyloxy)-2,2-bis[(benzoyloxy)methyl]propyl benzoate #
InChI=1/C33H28O8/c34-29(25-13-5-1-6-14-25)38-21-33(22-39-30(35)26-15-7-2-8-16-26,23-40-31(36)27-17-9-3-10-18-27)24-41-32(37)28-19-11-4-12-20-28/h1-20H,21-24H2