Interesting facts
Interesting Facts about 9-(Chloromethyl)anthracene
9-(Chloromethyl)anthracene is a fascinating compound with unique properties and applications in the field of chemistry. This compound is derived from anthracene, a polycyclic aromatic hydrocarbon, by the addition of a chloromethyl group. Here are some captivating insights into this compound:
- Versatile Intermediary: 9-(Chloromethyl)anthracene is often utilized as an intermediary in various chemical syntheses. It can serve as a precursor for the preparation of other functionalized anthracenes and derivatives.
- Photoactive Properties: With its extended π-conjugation from the anthracene backbone, this compound exhibits notable photophysical properties. It can absorb light, making it useful in studies concerning photochemistry and photophysics.
- Application in Materials Science: The chloromethyl group allows for further modification, enabling the incorporation of various functional groups that can lead to innovative materials with enhanced electronic properties.
- Research Relevance: Scientists have shown interest in this compound due to its potential applications in organic electronics and optoelectronic devices, such as organic light-emitting diodes (OLEDs).
- Health and Safety Considerations: As with many chlorinated compounds, caution should be observed in handling due to potential risks, including toxicity. Adequate safety protocols must be followed during research and experimentation.
In summary, 9-(Chloromethyl)anthracene is not just another compound; it's a gateway to explore the fascinating world of anthracene derivatives and their applications in modern chemistry. As the famous chemist Linus Pauling once stated, "The best way to have a good idea is to have a lot of ideas." This compound exemplifies how creativity in synthesis can lead to innovative discoveries.
Synonyms
9-(Chloromethyl)anthracene
24463-19-2
9-Chloromethylanthracene
Anthracene, 9-(chloromethyl)-
8C4ZDD4KUV
ANTHRACENE, 9-CHLOROMETHYL-
NSC-241165
DTXSID00179220
RefChem:107700
DTXCID30101711
246-274-7
9-Anthracenylmethyl chloride
MFCD00001263
C15H11Cl
ICR 448
9-Chloromethyanthracene
9-chloromethyl-anthracene
CCRIS 7993
EINECS 246-274-7
NSC 241165
BRN 1873394
9-CHLOROMETHYL ANTHRACENE
9-Chlormethyl-anthracen
UNII-8C4ZDD4KUV
MLS001335875
SCHEMBL592824
SCHEMBL2369643
CHEMBL1446266
SCHEMBL30350011
PCVRSXXPGXRVEZ-UHFFFAOYSA-
HMS2230A23
HMS3369G12
CS-D0568
STR05826
NSC241165
9-(Chloromethyl)anthracene, >=98%
AKOS015850544
SB66840
NCGC00246996-01
SMR000857350
SY001551
DB-046455
A5502
C1046
NS00027668
ST51039929
9-Chloromethylanthracene [for HPLC Labeling]
F14755
463C192
A928450
F788348
9-(Chloromethyl)anthracene, suitable for fluorescence, BioReagent, >=97.0% (AT)
InChI=1/C15H11Cl/c16-10-15-13-7-3-1-5-11(13)9-12-6-2-4-8-14(12)15/h1-9H,10H2
Solubility of 9-(chloromethyl)anthracene
The solubility of 9-(chloromethyl)anthracene, a chlorinated derivative of anthracene, can be better understood through a few key points:
In summary, while 9-(chloromethyl)anthracene has limited solubility in polar solvents like water, its solubility can be enhanced in nonpolar organic solvents, highlighting the importance of solvent choice in chemical processes.