CAS 612-60-2

7-Methylquinoline

Description:

7-Methylquinoline is an organic compound belonging to the quinoline family, characterized by a bicyclic structure that consists of a benzene ring fused to a pyridine ring. Its molecular formula is C10H9N, indicating the presence of ten carbon atoms, nine hydrogen atoms, and one nitrogen atom. This compound typically appears as a yellowish liquid or solid, depending on the temperature and purity. 7-Methylquinoline is known for its aromatic properties and exhibits a range of chemical reactivity, including electrophilic substitution due to the presence of the nitrogen atom in the pyridine ring. It is used in various applications, including as a building block in organic synthesis, in the production of dyes, and as a potential ligand in coordination chemistry. Additionally, 7-methylquinoline has been studied for its biological activities, including antimicrobial and antitumor properties. As with many organic compounds, proper handling and safety precautions are essential due to potential toxicity and environmental impact.

Formula: C₁₀H₉N

InChI: InChI=1/C10H9N/c1-8-4-5-9-3-2-6-11-10(9)7-8/h2-7H,1H3

InChI key: InChIKey=KDYVCOSVYOSHOL-UHFFFAOYSA-N

SMILES: CC1=CC2=C(C=C1)C=CC=N2

Synonyms:

• Ai3-00850
• Brn 0110317
• Ccris 2895
• Nsc 65665
• Quinoline, 7-methyl-
• m-Toluquinoline
• 5-20-07-00402 (Beilstein Handbook Reference)
• 7-Methylquinoline
• 7-METHYLQUINOLINE, (CONTAINS-20% 5-FORM) 75+%
• 7-Methylquinoline,97%
• Quinolinol,7-methyl-
• 7-METHYLQUINOLINE: TECH., 70%
• 7-methyquinoline
• 7-Methylquinoline (contains-25% 5-form)
• 7-Methylquinoline, tech. 70%, remainder mainly 5-isomer
• 7-methyl-quinolin
• 7-Methylquinolinol
• 7-Methylquinoline,tech.70%
• 7-Methylquiuoline

7-Methylquinoline (contains 25% 5-form at maximum)

CAS: 612-60-2

Formula: C₁₀H₉N

Purity: >75.0%(GC)

Color and Shape: Colorless to Light orange to Yellow clear liquid

Molecular weight: 143.19

Ref: 3B-M0417

7-Methylquinoline

CAS: 612-60-2

Formula: C₁₀H₉N

Purity: >98.0%(GC)

Color and Shape: White or Colorless to Almost white or Almost colorless powder to lump to clear liquid

Molecular weight: 143.19

Ref: 3B-M1180

7-Methylquinoline, 97%

CAS: 612-60-2

7-methylquinoline has been bioassayed as tumor initiator on the skin of Sencar mice. 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

Formula: C₁₀H₉N

Purity: 97%

Color and Shape: Pale yellow, Low melting solid / liquid

Molecular weight: 143.19

Ref: 02-042475

7-Methylquinoline

CAS: 612-60-2

7-Methylquinoline

Formula: C₁₀H₉N

Purity: 97%

Color and Shape: brown low melting solid

Molecular weight: 143.19g/mol

Ref: 54-OR911658

7-Methylquinoline

Controlled Product

CAS: 612-60-2

Formula: C₁₀H₉N

Color and Shape: Neat

Molecular weight: 143.185

Ref: 04-C20848750

7-Methylquinoline

CAS: 612-60-2

Formula: C₁₀H₉N

Purity: 95.0%

Color and Shape: Liquid

Molecular weight: 143.189

Ref: 10-F093281

m-Toluquinoline

Controlled Product

CAS: 612-60-2

Applications m-Toluquinoline is a reagent used in the preparation of diarylmethylpiperazines as potent opioid receptor agonists with improved side effects. Also used in the preparation of novel pyrazine compounds derived from 2-phenylquinolin-7-yl which act as potent insulin-like growth factor-I receptor inhibitors.
References Plobeck, N. et al.: J. Med. Chem., 43, 3878 (2000); Mulvihill, M. et al.: Bioorg Med. Chem. Lett., 16, 1359 (2008);

Formula: C₁₀H₉N

Color and Shape: Off-White

Molecular weight: 143.185

Ref: TR-T536555

7-Methylquinoline

CAS: 612-60-2

7-Methylquinoline is an organic compound that can be used to synthesize antimalarial drugs. It is a quinoline derivative with a methyl group at the 7th position. The structure of 7-methylquinoline contains a nitrogen atom and hydrogen atoms, which are bonded to fluorine, chlorine, and bromine atoms. This molecule has been shown to be stable in the presence of Friedel-Crafts catalysts and chloride ions. The reaction mechanism for 7-methylquinoline is intramolecular hydrogen transfer from the chloroform molecule to the quinoline ring system. The formation rate for this compound is slow because it requires two steps: nucleophilic substitution and electrophilic addition reactions.

Formula: C₁₀H₉N

Purity: Min. 95%

Molecular weight: 143.19 g/mol

Ref: 3D-FM40554