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9-Methylacridine
[CAS# 611-64-3]

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Identification
Classification Chemical reagent >> Organic reagent >> Tricyclic compound
Name 9-Methylacridine
Synonyms NSC 1234
Molecular Structure CAS # 611-64-3, 9-Methylacridine, NSC 1234
Molecular Formula C14H11N
Molecular Weight 193.24
CAS Registry Number 611-64-3
EC Number 210-272-4
SMILES CC1=C2C=CC=CC2=NC3=CC=CC=C13
Properties
Solubility Practically insoluble (0.039 g/L) (25 ºC), Calc.*
Density 1.155±0.06 g/cm3 (20 ºC 760 Torr), Calc.*
Melting point 129-130 ºC**
Index of Refraction 1.703, Calc.*
Boiling Point 361.9±11.0 ºC (760 mmHg), Calc.*
Flash Point 160.0±11.9 ºC, Calc.*
* Calculated using Advanced Chemistry Development (ACD/Labs) Software V11.02 (©1994-2014 ACD/Labs)
** Tsvelikhovsky, Dmitry; Journal of the American Chemical Society 2010, V132(40), P14048-14051.
Safety Data
Hazard Symbols symbol   GHS07 Warning    Details
Hazard Statements H315-H319-H335    Details
Precautionary Statements P261-P264-P264+P265-P271-P280-P302+P352-P304+P340-P305+P351+P338-P319-P321-P332+P317-P337+P317-P362+P364-P403+P233-P405-P501    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Skin irritationSkin Irrit.2H315
Eye irritationEye Irrit.2H319
Specific target organ toxicity - single exposureSTOT SE3H335
SDS Available
up Discovory and Applicatios
9-Methylacridine is a chemical compound belonging to the class of acridines, which are aromatic compounds containing a nitrogen atom within a three-ring structure. It consists of a methyl group attached to the ninth position of the acridine ring system. This modification of the acridine structure has significant implications for the chemical properties and reactivity of the molecule. 9-Methylacridine was first synthesized in the mid-20th century during the exploration of substituted acridines, a class of compounds known for their diverse chemical reactivity and biological activities. Since its discovery, 9-methylacridine has been studied for its applications in organic synthesis, material science, and medicinal chemistry.

One of the main applications of 9-methylacridine lies in its use as an intermediate in organic synthesis. Due to its unique chemical structure, it is a valuable building block for the synthesis of more complex compounds. 9-Methylacridine can participate in a variety of reactions, including nucleophilic substitution, electrophilic aromatic substitution, and other types of functional group transformations. These reactions enable the synthesis of other acridine derivatives, which are used in the production of dyes, agrochemicals, and pharmaceuticals. Its ability to form derivatives with various functional groups makes it a versatile compound in synthetic chemistry.

In addition to its use in organic synthesis, 9-methylacridine has found applications in the field of medicinal chemistry. Acridine derivatives, including 9-methylacridine, are known for their antimicrobial, anticancer, and antimalarial properties. The structure of 9-methylacridine allows it to interact with biological systems in ways that can inhibit the growth of pathogens or cancer cells. Researchers have explored the potential of 9-methylacridine and its derivatives as therapeutic agents, particularly in the development of drugs aimed at treating cancer and infectious diseases. Acridine-based compounds can intercalate into DNA, affecting the replication process, which makes them useful as chemotherapeutic agents.

9-Methylacridine has also been studied for its role in the development of optoelectronic materials. The presence of a nitrogen atom in the acridine ring and the methyl group at the ninth position can influence the electronic properties of the molecule, making it a candidate for use in light-emitting devices, organic semiconductors, and other electronic applications. The compound’s ability to absorb and emit light at specific wavelengths makes it useful in the design of organic light-emitting diodes (OLEDs) and organic solar cells. These materials are of particular interest due to their potential for use in flexible electronics and energy-efficient devices.

Moreover, 9-methylacridine has been investigated for its potential use in fluorescence-based sensors and detection systems. Its fluorescence properties, when exposed to certain wavelengths of light, can be harnessed for sensing applications, such as the detection of specific metal ions or other environmental pollutants. By modifying the structure of 9-methylacridine, researchers have been able to design sensors that can selectively bind to target molecules, providing a useful tool for environmental monitoring and diagnostic applications.

In conclusion, 9-methylacridine is a valuable chemical compound with a wide range of applications in organic synthesis, medicinal chemistry, material science, and sensor technology. Its unique structure allows it to participate in various chemical reactions and interact with biological systems, making it an important building block for the development of new therapeutic agents and functional materials. As research continues to explore its potential, 9-methylacridine is likely to remain an important compound in both academic and industrial settings.
Market Analysis Reports
List of Reports Available for 9-Methylacridine
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