Interesting facts
Interesting Facts about 9,10-bis(chloromethyl)anthracene
9,10-bis(chloromethyl)anthracene is a fascinating organic compound with a unique structure and properties that make it a subject of interest in various fields of chemistry. Here are some engaging aspects about this compound:
- Polycyclic Aromatic Hydrocarbon (PAH): This compound is categorized as a PAH, characterized by multiple fused benzene rings. These types of compounds are significant in atmospheric chemistry and are often studied for their environmental impact.
- Chloromethyl Groups: The presence of two chloromethyl groups on the anthracene structure enhances its reactivity and is instrumental in a variety of chemical reactions, such as Friedel-Crafts alkylation. This makes it a versatile intermediate for synthesizing larger, more complex molecules.
- Photophysical Properties: 9,10-bis(chloromethyl)anthracene exhibits interesting photophysical behaviors, which can be leveraged in the development of optical materials and sensors. Its ability to absorb and emit light opens up possibilities in applications like fluorescence spectroscopy.
- Research Applications: This compound has garnered attention in medicinal chemistry for its potential role in drug development. Due to its ability to form covalent bonds with biological molecules, it is investigated for its anticancer properties.
- Toxicity Awareness: Like many chlorinated compounds, it is vital to handle 9,10-bis(chloromethyl)anthracene with care due to its potential toxicity. This fact emphasizes the importance of safety protocols in labs when working with reactive chemicals.
In summary, 9,10-bis(chloromethyl)anthracene is an intriguing compound with a variety of applications and implications. Its unique structure enables diverse research opportunities while also necessitating responsible handling in laboratory settings.
Synonyms
9,10-Bis(chloromethyl)anthracene
ANTHRACENE, 9,10-BIS(CHLOROMETHYL)-
ICR-450
CCRIS 948
NSC 81650
BRN 2055024
ICR 450
DTXSID1065059
UOSROERWQJTVNU-UHFFFAOYSA-
4-05-00-02330 (Beilstein Handbook Reference)
DTXCID8032831
677-977-0
inchi=1/c16h12cl2/c17-9-15-11-5-1-2-6-12(11)16(10-18)14-8-4-3-7-13(14)15/h1-8h,9-10h2
uosroerwqjtvnu-uhfffaoysa-n
10387-13-0
9,10-Di(chloromethyl)anthracene
74QY2YM6ZQ
9,10-Bis-chloromethyl-anthracene
NSC-81650
C16H12Cl2
MFCD00045388
UNII-74QY2YM6ZQ
NCIOpen2_004345
9,10-dichloromethylanthracene
SCHEMBL187486
Anthracene,10-bis(chloromethyl)-
9,10-Bis-(chloromethyl)anthracene
ALBB-033467
BCP15398
NSC81650
WLN: L C666J B1G I1G
Bis(chloromethyl)anthracene, 9,10-
STK364704
AKOS000508101
AC-5802
CS-W004459
AS-36693
9 pound not10-bis(chloromethyl)anthracene
DB-014683
B1327
NS00125741
ST50245111
Solubility of 9,10-bis(chloromethyl)anthracene
9,10-bis(chloromethyl)anthracene is an intriguing compound when it comes to its solubility characteristics. Understanding the solubility behavior of this compound is essential for various applications, especially in organic chemistry and materials science.
Solubility Characteristics
When considering the solubility of 9,10-bis(chloromethyl)anthracene, it is important to note:
As noted, the solubility of 9,10-bis(chloromethyl)anthracene can be summarized as follows:
In conclusion, the solubility behavior of 9,10-bis(chloromethyl)anthracene is crucial for its use in various chemical processes and applications. Its solubility profile is mainly influenced by the solvent polarity, making it a prime candidate for studies involving nonpolar environments.