93873-16-6

Basic information

• Product Name: 1-methyl-3-[1-(2-phenylhydrazino)ethylidene]quinoline-2,4(1H,3H)-dione
• CAS NO: 93873-16-6
• Molecular Formula: C₁₈H₁₇N₃O₂
• Molecular Weight: 307.3465
• Mol File: 93873-16-6.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 385°C at 760 mmHg
• Flash Point: 186.6°C
• Density: 1.289g/cm³
• Vapor Pressure: 3.93E-06mmHg at 25°C
• Refractive Index: 1.665
• CAS DataBase Reference: 1-methyl-3-[1-(2-phenylhydrazino)ethylidene]quinoline-2,4(1H,3H)-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 1-methyl-3-[1-(2-phenylhydrazino)ethylidene]quinoline-2,4(1H,3H)-dione(93873-16-6)
• EPA Substance Registry System: 1-methyl-3-[1-(2-phenylhydrazino)ethylidene]quinoline-2,4(1H,3H)-dione(93873-16-6)

Safety Data

• Hazardous Substances Data: 93873-16-6(Hazardous Substances Data)

Usage

Explanation

This is the chemical name of the compound, which describes its structure and components.

Explanation

The compound belongs to the quinoline class, which is a group of nitrogen-containing aromatic compounds.

Explanation

The central structure of the compound is a quinoline ring, which is a tricyclic aromatic system containing two benzene rings fused to a pyridine ring.

Explanation

The quinoline core structure has additional substituents attached to it, including a methyl group (-CH3), a hydrazino group (-NHNH2), and an ethylidene group (-CH=CH2).

Explanation

The compound has potential biological activity, which means it may interact with biological systems and have pharmacological effects.

Explanation

Due to its potential biological activity, the compound may be used in the research and development of new pharmaceuticals and drugs.

Explanation

More research and testing are needed to fully comprehend the properties, potential applications, and limitations of this chemical compound.

Classification

Quinoline class of chemicals

Core structure

Quinoline

Substituents

Methyl group, hydrazino group, and ethylidene group

Biological activity

Potential

Applications

Pharmaceutical research and drug development

Safety precautions

Handle with care, follow proper safety protocols

Further research

Necessary to understand properties and applications

Upstream product

• 54289-76-8 3-acetyl-4-hydroxy-1-methyl-2(1H)-quinolone 
• 100-63-0 phenylhydrazine 
• 26138-64-7 4-hydroxy-3-acetyl-1H-quinoline-2-one 

Downstream Products

• 71814-52-3 3,5-dimethyl-1-phenyl-1,5-dihydro-4H-pyrazolo[4,3-c]quinolin-4-one 
• 938436-04-5 3-(4-hydroxy-1-methyl-1,2-dihydro-2-oxoquinolin-3-yl)-1-phenyl-1H-pyrazole-4-carbaldehyde 
• 685891-37-6 1-methyl-2-oxo-3-[1-(phenylhydrazono)ethyl]-1,2-dihydroquinolin-4-yl 4-methylbenzenesulfonate 

Relevant articles and documents

Synthesis and antioxidant properties of some novel 1,3,4,2-oxadiazaphosphepino[6,7-c]quinolinones and pyrazolo[3,4:4′,3′]quinolino[5,1-c][1,4,2]oxazaphosphinine

A series of novel 1,3,4,2-oxadiazaphosphepino[6,7-c]quinolinones 3–5, 9, and 11 have been synthesized from treatment of 4-hydroxy-1-methyl-3-[1-(2-phenylhydrazinylidene)ethyl]quinolin-2(1H)-one (2) with some phosphorus sulfides, diethyl phosphite and phen

Synthesis, crystal structure and spectroscopic studies of 3- hydrazono- and 3-hydroxyiminoquinolin-2-ones

3-(Hydrazonoethyl)quinolinones 6-11, 13 and 3- (hydroxyiminoethyl)quinolinones 14, 15 are prepared by a condensation reaction of 3-acetylquinolinones 4, 5 with a variety of 1,2-(bis)nucleophiles. The structures of the isolated compounds have been elucidated using 1H and 13C nmr spectroscopy. X-ray diffraction studies of compound 14 were also performed.