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9-(Bromomethyl)anthracene

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Identification
Molecular formula
C15H11Br
CAS number
1711-17-7
IUPAC name
9-(bromomethyl)anthracene
State
State

At room temperature, 9-(bromomethyl)anthracene is in a solid state.

Melting point (Celsius)
62.00
Melting point (Kelvin)
335.15
Boiling point (Celsius)
425.50
Boiling point (Kelvin)
698.50
General information
Molecular weight
273.16g/mol
Molar mass
273.1570g/mol
Density
1.5010g/cm3
Appearence

The compound typically appears as a light yellow to orange crystalline solid.

Comment on solubility

Solubility of 9-(Bromomethyl)anthracene

9-(Bromomethyl)anthracene, with the chemical formula C14H11Br, exhibits selective solubility characteristics that make it an interesting compound in the realm of organic chemistry.

When considering its solubility, one can note the following key points:

  • Polar vs. Non-Polar Solvents: 9-(Bromomethyl)anthracene tends to dissolve better in non-polar organic solvents. This is largely due to its hydrophobic anthracene backbone, which prefers environments where it can minimize interactions with water molecules.
  • Common Solvents: It shows solubility in solvents such as hexane and chloroform, where the non-polar interactions dominate, promoting good solvation.
  • Limited Water Solubility: Due to the presence of the bromomethyl group, it can exhibit limited solubility in polar solvents such as water. This limited solubility is attributed to the overall large and non-polar structure of the anthracene moiety.

To summarize, understanding the solubility of 9-(bromomethyl)anthracene highlights its interaction with different types of solvents, which is crucial for applications in organic synthesis and materials science. As noted, it is primarily soluble in non-polar solvents, making it favorable for various chemical reactions within that medium.

Interesting facts

Interesting Facts About 9-(Bromomethyl)anthracene

9-(Bromomethyl)anthracene is a fascinating chemical compound that showcases the diversity and complexity of polycyclic aromatic hydrocarbons. Here are some intriguing insights about it:

  • Structural Importance: As a derivative of anthracene, this compound features a bromomethyl group at the 9-position, which significantly affects its chemical reactivity and physical properties.
  • Reactivity: The presence of the bromomethyl group makes it a valuable intermediate in organic synthesis, allowing it to participate in various reactions, such as nucleophilic substitutions and coupling reactions.
  • Applications: Its unique structure has implications in materials science, particularly in the development of organic semiconductors, light-emitting diodes (LEDs), and photovoltaic devices.
  • Photophysical Properties: Compounds like this often exhibit interesting photophysical properties, making them suitable for studying the behavior of excited states and energy transfer processes in molecular systems.
  • Research Potential: The versatility of 9-(bromomethyl)anthracene in forming complex molecular architectures offers significant potential for research in fields such as nanotechnology, organic electronics, and medicinal chemistry.

In the words of a noted chemist, "Compounds like 9-(bromomethyl)anthracene remind us that the building blocks of nature often yield the most unexpected and innovative applications."

As we explore the vast landscape of polycyclic aromatic hydrocarbons, 9-(bromomethyl)anthracene serves as an excellent example of how modifications to a simple structure can lead to profound advancements in both science and technology.

Synonyms
9-(Bromomethyl)anthracene
2417-77-8
9-Bromomethylanthracene
ANTHRACENE, 9-BROMOMETHYL-
ICR 506
CCRIS 822
9JN2QR4LWJ
BRN 2049298
BROMOMETHYLANTHRACENE, 9-
DTXSID70178881
DTXCID30101372
803-482-8
C15H11Br
MFCD00096212
Anthracene, 9-(bromomethyl)-
9-bromomethyl-anthracene
UNII-9JN2QR4LWJ
SCHEMBL118514
KOWKPLCVFRHICH-UHFFFAOYSA-N
BBL100121
STK368189
AKOS005445194
CS-W009231
SB66830
DS-17268
FB180228
SY033909
DB-022238
A10862
EN300-7415857
InChI=1/C15H11Br/c16-10-15-13-7-3-1-5-11(13)9-12-6-2-4-8-14(12)15/h1-9H,10H