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Triphenylmethyl chloride

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Identification
Molecular formula
C19H15Cl
CAS number
76-83-5
IUPAC name
[chloro(diphenyl)methyl]benzene
State
State
At room temperature, triphenylmethyl chloride is typically found in a solid state, specifically as a crystalline powder. It is relatively stable but should be stored away from moisture due to its reactivity with water.
Melting point (Celsius)
112.00
Melting point (Kelvin)
385.15
Boiling point (Celsius)
377.00
Boiling point (Kelvin)
650.15
General information
Molecular weight
262.78g/mol
Molar mass
262.7710g/mol
Density
1.1990g/cm3
Appearence
Triphenylmethyl chloride appears as a white to pale yellow crystalline powder. It can sometimes be observed as colorless crystals depending on its purity.
Comment on solubility

Solubility of [chloro(diphenyl)methyl]benzene

[chloro(diphenyl)methyl]benzene, also known as a chlorinated aromatic compound, exhibits specific solubility characteristics that are essential to understand for various applications. The compound's solubility is largely influenced by its chemical structure, which incorporates both hydrophobic and polar elements.

In general, the solubility of [chloro(diphenyl)methyl]benzene can be analyzed in the following contexts:

  • Non-polar Solvents: This compound readily dissolves in non-polar solvents such as toluene or benzene due to its aromatic nature and hydrophobic characteristics.
  • Polar Solvents: Its solubility in polar solvents like water is minimal, as the compound does not mix well with polar molecules. This aligns with the principle of like dissolves like.
  • Temperature Dependence: The solubility may vary with temperature, where increased temperatures can often enhance solubility in non-polar solvents.

As a result, it is crucial to consider these factors when working with [chloro(diphenyl)methyl]benzene in both experimental and industrial settings. Understanding its solubility behavior aids in selecting appropriate solvents for reactions and extractions, thereby optimizing processes and ensuring safety protocols.

In conclusion, the solubility of [chloro(diphenyl)methyl]benzene is a vital property dictated by its chemical structure, significantly affecting its interactions and applications in various chemical environments.

Interesting facts

Interesting Facts about Chloro(diphenyl)methylbenzene

Chloro(diphenyl)methylbenzene, commonly referred to as a versatile organic compound, is a notable element in the field of synthetic organic chemistry. Its structure, which features a chloro group attached to a benzene ring with a diphenylmethyl functional group, opens the door to a variety of interesting properties and applications.

Key Applications

  • Synthesis Intermediates: This compound is often utilized as an intermediate in the synthesis of more complex organic molecules.
  • Pharmaceutical Research: Researchers have shown interest in its potential application in developing new pharmaceuticals due to its unique molecular structure.
  • Material Sciences: Chloro(diphenyl)methylbenzene is also explored for its properties in the creation of new materials, particularly those that require specific electronic features.

Chemical Properties

The presence of the chloro group not only affects its reactivity but also plays a crucial role in its ability to engage in various chemical transformations. As a halogenated compound, it exhibits different polarity and reactivity patterns compared to its non-halogenated counterparts.

Environmental Impact

While chloro(diphenyl)methylbenzene has valuable applications, it’s essential to be aware of its environmental implications. The chlorine atom can lead to concerns regarding stability and persistence in the environment, making it an important subject for studies focusing on environmental chemistry and toxicology.

Fun Fact

Did you know? The concept of using diphenyl groups in chemical synthesis has historical roots in the development of various dyes and polymers. This compound serves as a reminder of the rich history and transformative nature of organic chemistry!

In conclusion, chloro(diphenyl)methylbenzene stands out due to its multifaceted role in research and synthesis, highlighting the intricate balance between utility and environmental stewardship in chemical applications.

Synonyms
Triphenylmethyl chloride
76-83-5
Trityl chloride
CHLOROTRIPHENYLMETHANE
Triphenylchloromethane
(chloromethanetriyl)tribenzene
Methane, chlorotriphenyl-
triphenylmethylchloride
(chlorodiphenylmethyl)benzene
Benzene, 1,1',1''-(chloromethylidyne)tris-
[Chloro(diphenyl)methyl]benzene
1,1',1''-(Chloromethylidyne)trisbenzene
HSDB 2807
NSC 435
1D9GZ8QQXN
EINECS 200-986-4
BRN 0397363
DTXSID3052511
AI3-51298
NSC-435
MFCD00000813
TRITYL CHLORIDE [MI]
1,1',1''-(chloromethanetriyl)tribenzene
DTXCID7031084
4-05-00-02497 (Beilstein Handbook Reference)
1411984-26-3
triphenyl chloromethane
MFCD00284810
C19H15Cl
UNII-1D9GZ8QQXN
tritylchloride
trityl-chloride
TrtCl
trt-cl
TrCl
Cl-Trt
Ph3CCl
triphenymethylchloride
TPCM
chloro triphenylmethane
triphenylmethyl choride
Trityl Chloride Resin
3880-98-6
Chlorotriphenyl methane
Chlorotriphenyl-methane
Chlorotriphenylmethane (Trityl chloride)
triphenylmethyl-chloride
Trityl chloride, 97%
triphenyl methyl chloride
triphenyl-methyl chloride
triphenyl-methyl-chloride
(triphenyl)methyl chloride
SCHEMBL461
Chlorotriphenylmethane resin
diphenyl-phenyl-chloromethane
(chloro-diphenyl-methyl)benzene
CHEMBL261393
NSC435
BDBM23782
[Chloro(diphenyl)methyl]benzene #
STR01707
Tox21_303949
BBL100118
c0308
STK366821
AKOS005444080
Triphenylchloromethane; Trityl chloride
CS-W009020
FT01757
FT29918
CAS-76-83-5
Triphenylmethyl-containing compound, 11
NCGC00357183-01
BP-21049
Benzene,1',1''-(chloromethylidyne)tris-
1,1',1''-(chloromethylidyne)tris-benzene
Benzene, 1,1',1''(chloromethylidyne)tris
Benzene, 1,1',1"-(chloromethylidyne)tris-
NS00037847
EN300-21614
C93509
Benzene, 1,1',1''-(chloromethylidyne-13C)tris-
Q2790082
F0001-1923
Trityl chloride, purum, >=97.0% (HPLC), >=97.0% (AT)
Trityl chloride resin (100-200 mesh, 1% DVB, 1.2-2.0 mmol/g
Trityl chloride resin (200-400 mesh, 1% DVB, 1.2-2.0 mmol/g)
200-986-4