CAS 611-64-3

9-Methylacridine

Description:

9-Methylacridine is an organic compound belonging to the acridine family, characterized by a fused three-ring structure that includes a nitrogen atom. It is a pale yellow to brownish solid at room temperature and is known for its aromatic properties. The presence of the methyl group at the 9-position of the acridine ring system influences its chemical behavior, making it a potential candidate for various applications in organic synthesis and as a fluorescent probe. 9-Methylacridine is moderately soluble in organic solvents, such as ethanol and acetone, but has limited solubility in water. Its chemical reactivity is primarily attributed to the nitrogen atom, which can participate in various reactions, including electrophilic substitution and oxidation. Additionally, 9-Methylacridine exhibits photophysical properties, making it useful in studies related to fluorescence and photochemistry. Safety data indicates that it should be handled with care, as it may pose health risks upon exposure. Overall, 9-Methylacridine is a compound of interest in both academic research and industrial applications.

Formula: C₁₄H₁₁N

InChI: InChI=1/C14H11N/c1-10-11-6-2-4-8-13(11)15-14-9-5-3-7-12(10)14/h2-9H,1H3

InChI key: InChIKey=FLDRLXJNISEWNZ-UHFFFAOYSA-N

SMILES: CC=1C2=C(N=C3C1C=CC=C3)C=CC=C2

Synonyms:

• 5-Methylacridine
• 5-Methylacridine (European)
• 9-Methylakridin
• 9-Methylakridin [Czech]
• Acridine, 9-methyl-
• Brn 0133084
• Nsc 1234
• 9-Methylacridine
• 5-20-08-00253 (Beilstein Handbook Reference)
• 9-Methylacridine
• 9-Methylacridine, 99+%
• 9-Methylacridin
• 9-Methylacridine, 99+% 1GR
• 9-methyl-acridin

9-Methylacridine

CAS: 611-64-3

Formula: C₁₄H₁₁N

Purity: >97.0%(GC)

Color and Shape: Light yellow to Brown to Dark green powder to crystal

Molecular weight: 193.25

Ref: 3B-M1237

9-Methylacridine, 96%

CAS: 611-64-3

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci

Formula: C₁₄H₁₁N

Purity: 96%

Color and Shape: Yellow to brown, Powder or crystalline powder

Molecular weight: 193.25

Ref: 02-H33718

9-Methylacridine

CAS: 611-64-3

Heterocyclic compounds with nitrogen hetero-atom(s) only, aromatic or modified aromatic, nesoi

Formula: C₁₄H₁₁N

Color and Shape: Yellow Powder

Molecular weight: 193.08915

Ref: 45-1424084

9-Methylacridine

CAS: 611-64-3

Formula: C₁₄H₁₁N

Purity: 98%

Color and Shape: Solid

Molecular weight: 193.2438

Ref: IN-DA003NLF

9-Methylacridine

CAS: 611-64-3

9-Methylacridine

Purity: 98%

Molecular weight: 193.24g/mol

Ref: 54-OR56794

9-Methyl Acridine

CAS: 611-64-3

Formula: C₁₄H₁₁N

Color and Shape: Yellowish-Brown Solid

Molecular weight: 193.25

Ref: 4Z-A-141003

9-Methylacridine

Controlled Product

CAS: 611-64-3

Formula: C₁₄H₁₁N

Color and Shape: Neat

Molecular weight: 193.24

Ref: 86-MM0076.09

9-Methylacridine

CAS: 611-64-3

9-Methylacridine is an environmentally sensitive fluorescent probe that can couple with carboxylic acid molecules.

Formula: C₁₄H₁₁N

Color and Shape: Solid

Molecular weight: 193.24

Ref: TM-T64963

9-Methylacridine

CAS: 611-64-3

Purity: 95.0%

Color and Shape: Solid

Molecular weight: 193.24899291992188

Ref: 10-F339995

Carbamazepine EP Impurity B

CAS: 611-64-3

Formula: C₁₄H₁₁N

Molecular weight: 193.25

Ref: ST-EA-CP-C8002

9-Methylacridine

Controlled Product

CAS: 611-64-3

Applications 9-Methylacridine is an derivative of Acridine (A190900), a quinoline derivative used as manufacturing dyes and as an intermediate for the synthesis of antileishmanial agents.
References Pathak, D. et al.: Pharma Chemica, 3, 239 (2011); Mathieu, O. et al.: Xenobiotica, 41, 91 (2011); Rubbo, S.D. et al.: Br. J. Exp. Pathol., 28, 1 (1947);

Formula: C₁₄H₁₁N

Color and Shape: Neat

Molecular weight: 193.24

Ref: TR-M285050

9-methylacridine

CAS: 611-64-3

9-Methylacridine is a chemical compound that is a member of the acridine family. It has shown anticancer activity in animal studies and also has been used as an immunosuppressant. 9-Methylacridine can be synthesized by reacting sodium carbonate with intramolecular hydrogen, which is then purified by Langmuir adsorption isotherm. The antiviral effect of 9-methylacridine was tested on herpes simplex virus and it was found that this compound inhibited the transfer reactions of viral DNA to host cells, leading to inhibition of viral replication. Studies have also shown that 9-methylacridine has anti-inflammatory effects against caproic acid and malonic acid in rats. One study found that 9-methylacridine inhibits the cationic polymerization and biological samples are usually anhydrous sodium chloride or human serum.

Formula: C₁₄H₁₁N

Purity: Min. 95%

Molecular weight: 193.24 g/mol

Ref: 3D-FM59402