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Triphenylmethyl bromide

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Identification
Molecular formula
C19H15Br
CAS number
996-47-8
IUPAC name
[bromo(diphenyl)methyl]benzene
State
State

At room temperature, Triphenylmethyl bromide is generally in a solid state. It exists as crystalline solids or powder form, which is stable under standard conditions of temperature and pressure.

Melting point (Celsius)
95.00
Melting point (Kelvin)
368.15
Boiling point (Celsius)
283.00
Boiling point (Kelvin)
556.15
General information
Molecular weight
339.25g/mol
Molar mass
339.2450g/mol
Density
1.3880g/cm3
Appearence

Triphenylmethyl bromide appears as a colorless or slightly yellow crystalline solid. It is sensitive to air and moisture, which may cause degradation or discoloration. Fine needles or crystalline powder can form depending on the conditions of crystallization.

Comment on solubility

Solubility of [bromo(diphenyl)methyl]benzene

[bromo(diphenyl)methyl]benzene, also known as benzylic bromide, is a compound that exhibits specific solubility characteristics influenced by its structure and the presence of bromine substituents. Its solubility can be described in the following ways:

  • Solvent Polarity: It is generally more soluble in organic solvents such as ethanol, ether, and benzene due to its non-polar characteristics. The presence of non-polar diphenyl groups enhances its affinity for non-polar solvents.
  • Water Solubility: This compound is expected to have low solubility in water. The bulky nature of the diphenyl groups and the bromine atom limit its interactions with polar water molecules.
  • Temperature Effects: As with many organic compounds, solubility can increase with temperature, making it easier to dissolve in hot solvents compared to cold ones.

In conclusion, [bromo(diphenyl)methyl]benzene is primarily soluble in organic solvents and demonstrates limited solubility in water, highlighting the importance of choosing the right solvent for applications involving this compound.

Interesting facts

Interesting Facts About [bromo(diphenyl)methyl]benzene

[bromo(diphenyl)methyl]benzene, also known as a brominated derivative of diphenylmethane, is an intriguing compound in the realm of organic chemistry. This compound plays a significant role in various chemical reactions and applications.

Chemical Characteristics and Reactivity

Here are some highlighted facts regarding its characteristics and reactivity:

  • Bromination Reaction: The presence of the bromine atom facilitates electrophilic substitution reactions, allowing for further functionalization and synthesis of complex organic molecules.
  • Stability: Compared to other halogenated compounds, the bromo group contributes to the stability of the molecule, making it a useful intermediate in synthetic pathways.
  • Applications: It is utilized in the synthesis of pharmaceuticals, agrochemicals, and various organic compounds, showcasing its versatility.

Chemical Significance

This compound not only highlights the utility of bromine in organic synthesis but also serves as a building block in the construction of more complex molecules. Some notable aspects include:

  • It can act as a cross-coupling reagent, enabling the formation of carbon-carbon bonds, which is essential in constructing larger organic frameworks.
  • As a key intermediate, it is pivotal in the production of aromatic compounds, which are vital in industrial chemistry.

In the Laboratory

When handling this compound, it is crucial to consider safety measures due to the reactive nature of brominated compounds. Always ensure to:

  • Work in a well-ventilated area.
  • Utilize appropriate personal protective equipment (PPE).
  • Follow all safety protocols when disposing of any chemical waste.

In conclusion, [bromo(diphenyl)methyl]benzene represents a fascinating intersection of reactivity, stability, and practical applications within organic chemistry. Its role as a versatile building block cannot be overstated, making it an essential compound for chemists and researchers alike.

Synonyms
Bromotriphenylmethane
Triphenylmethyl bromide
596-43-0
Trityl bromide
METHANE, BROMOTRIPHENYL-
Benzene, 1,1',1''-(bromomethylidyne)tris-
2-Bromo-1,1,1-triphenylethane
EINECS 209-884-4
EWY6H8D4L5
NSC 66464
BRN 1878494
AI3-51274
NSC-66464
DTXSID4060494
4-05-00-02500 (Beilstein Handbook Reference)
1,1',1''-(BROMOMETHYLIDYNE)TRIS(BENZENE)
Methane, bromotriphenyl
DTXCID7042647
Benzene, 1,1',1''(bromomethylidyne)tris
209-884-4
inchi=1/c19h15br/c20-19(16-10-4-1-5-11-16,17-12-6-2-7-13-17)18-14-8-3-9-15-18/h1-15
(bromomethanetriyl)tribenzene
Triphenylbromomethane
(bromodiphenylmethyl)benzene
[Bromo(diphenyl)methyl]benzene
triphenylmethylbromide
.alpha.-Bromotriphenylmethane
MFCD00000120
TRITYLBROMIDE
SCHEMBL263
UNII-EWY6H8D4L5
Bromotriphenylmethane, 98%
CHEMBL270127
BDBM23783
[Bromo(diphenyl)methyl]benzene #
NSC66464
AKOS009086994
Triphenylmethyl-containing compound, 12
Benzene,1',1''-(bromomethylidyne)tris-
BS-17270
DB-053433
CS-0137175
NS00034207
T0512
EN300-24072
F11172