CAS 611-34-7

5-Aminoquinoline

Description:

5-Aminoquinoline is an organic compound characterized by a quinoline structure with an amino group positioned at the 5th carbon. Its molecular formula is C9H8N2, indicating the presence of nine carbon atoms, eight hydrogen atoms, and two nitrogen atoms. This compound typically appears as a yellow to brown solid and is known for its aromatic properties, which contribute to its stability and reactivity. 5-Aminoquinoline is soluble in organic solvents such as ethanol and dimethyl sulfoxide, but its solubility in water is limited. It is often utilized in various chemical syntheses, including the production of dyes, pharmaceuticals, and agrochemicals. Additionally, 5-aminoquinoline exhibits biological activity, making it of interest in medicinal chemistry for potential applications in treating diseases. Its reactivity can be attributed to the presence of the amino group, which can participate in various chemical reactions, including electrophilic substitutions and coupling reactions. Safety precautions should be observed when handling this compound, as it may pose health risks if ingested or inhaled.

Formula: C₉H₈N₂

InChI: InChI=1S/C9H8N2/c10-8-4-1-5-9-7(8)3-2-6-11-9/h1-6H,10H2

InChI key: InChIKey=XMIAFAKRAAMSGX-UHFFFAOYSA-N

SMILES: NC=1C2=C(C=CC1)N=CC=C2

Synonyms:

• (Quinolin-5-yl)amine
• 5-Quinolinamine
• 5-Quinolylamine
• Asischem Z74663
• Iflab-Bb F2124-0039
• NSC 170619
• NSC 27982
• Quinolin-5-amine
• Quinoline, 5-amino-
• Quinoline-5-amine
• Timtec-Bb Sbb010065

5-Aminoquinoline, 99%

CAS: 611-34-7

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: C₉H₈N₂

Purity: 99%

Color and Shape: Yellow to brown, Powder

Molecular weight: 144.18

Ref: 02-L19628

Quinolin-5-amine

CAS: 611-34-7

Formula: C₉H₈N₂

Purity: 96%

Color and Shape: Solid

Molecular weight: 144.1732

Ref: IN-DA003MEO

5-Aminoquinoline

CAS: 611-34-7

Formula: C₉H₈N₂

Molecular weight: 144.18

Ref: 7W-GK5235

5-Aminoquinoline

CAS: 611-34-7

5-Aminoquinoline

Formula: C₉H₈N₂

Purity: 97%

Color and Shape: light brown to brown solid

Molecular weight: 144.17g/mol

Ref: 54-OR4011

5-Aminoquinoline

CAS: 611-34-7

Formula: C₉H₈N₂

Purity: >99.0%(T)

Color and Shape: White to Yellow to Orange powder to crystalline

Molecular weight: 144.18

Ref: 3B-A0959

5-Aminoquinoline

Controlled Product

CAS: 611-34-7

Applications Intermediate in the preparation of P2X7 antagonists
References Donnelly-Roberts, D., et al.: Neuropharmacol., 56, 223 (2009), Perez-Medrano, A., et al.: J. Med. Chem., 52, 3366 (2009),

Formula: C₉H₈N₂

Color and Shape: Neat

Molecular weight: 144.17

Ref: TR-A629165

5-Aminoquinoline

CAS: 611-34-7

Formula: C₉H₈N₂

Purity: 96%

Color and Shape: Solid

Molecular weight: 144.177

Ref: 10-F048215

5-Aminoquinoline

CAS: 611-34-7

5-Aminoquinoline (5-AQ) is a chemical compound that was originally synthesized in the 1930s. 5-AQ is a trifluoroacetic acid derivative of quinoline, which has been used as a photographic developer and an agent for the removal of silver from photographic film. This molecule also has a fluorescence property, which can be seen when irradiated by light with a wavelength greater than 350 nm. A hydrogen bond exists between the hydroxyl group and the nitrogen atom of the amine group in 5-AQ. The reaction mechanism for 5-AQ is believed to involve the diazonium salt intermediate, which reacts with silver ions to form silver diazonide and free ammonia.
5-AQ is insoluble in water but soluble in organic solvents such as acetone or alcohol. It reacts with trifluoroacetic acid to form a precipitate, which may be removed by filt

Formula: C₉H₈N₂

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 144.17 g/mol

Ref: 3D-FA15583