7-Amino-4-methylquinolin-2(1H)-one | CAS 19840-99-4

Name: 7-Amino-4-methylquinolin-2(1H)-one
Brand: BOC Sciences
Rating: 5 (1 reviews)

Catalog Number	A17-0041
Category	Laser Dyes
Molecular Formula	C10H10N2O
Molecular Weight	174.20

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Product Introduction

This quinolinone fluorescent probe features strong emission and broad chemical compatibility for sensor development. Buy fluorescent dyes online for FRET, live-cell imaging, and molecular diagnostics.

Chemical Information
Application

Synonyms	Carbostyril 124;7-amino-4-methyl-1H-quinolin-2-one; 7-amino-4-methyl-1H-quinolin-2-one
IUPAC Name	7-amino-4-methyl-1H-quinolin-2-one
Canonical SMILES	CC1=CC(=O)NC2=C1C=CC(=C2)N
InChI	InChI=1S/C10H10N2O/c1-6-4-10(13)12-9-5-7(11)2-3-8(6)9/h2-5H,11H2,1H3,(H,12,13)
InChIKey	MJXYFLJHTUSJGU-UHFFFAOYSA-N
Density	1.223 g/cm³
Appearance	Off-white to light beige solid
Boiling Point	417.6 °C at 760 mmHg
Melting Point	>270 °C (dec.)
LogP	2.41220

7-Amino-4-methylquinolin-2(1H)-one, a versatile organic compound, finds significant applications in diverse bioscience fields.

Pharmaceutical Research: Serving as a valuable scaffold for new therapeutic agents, 7-Amino-4-methylquinolin-2(1H)-one stands at the forefront of drug discovery. Its distinctive quinoline structure positions it as an ideal candidate for combating bacterial infections and cancer. Researchers delve into its modifications, seeking to amplify biological activity while mitigating potential side effects, propelling the realm of pharmaceutical innovation.

Chemical Synthesis: Operating as a pivotal intermediate in molecular synthesis, this compound plays a crucial role in generating complex molecules. Frequently utilized in crafting heterocyclic compounds and other pharmacologically active agents, it offers chemists a canvas to introduce diverse functional groups, yielding derivatives with a wide array of chemical properties and prospective applications.

Fluorescent Probes: The inherent fluorescent characteristics of 7-Amino-4-methylquinolin-2(1H)-one render it an indispensable asset in the realm of fluorescent probe development. These probes, integral to various imaging methodologies, illuminate cellular components and biological processes, affording researchers a real-time glimpse into cellular dynamics, protein interactions, and other phenomena.

Biochemical Assays: Versatile in its application, 7-Amino-4-methylquinolin-2(1H)-one emerges as a critical substrate and reagent in biochemical assays. Its reactive nature enables participation in enzymatic reactions, facilitating the detection of specific enzyme activities. These assays play a pivotal role in diagnostics, drug screening, and enzymology research, offering invaluable insights into the biochemical underpinnings of biological systems.