78333-68-3

Basic information

• Product Name: 1H-Indene-5-carboxylic acid, 2,3-dihydro-2-(3-hydroxy-2-quinolinyl)-1,3-dioxo-, 2-ethoxyethyl ester
• Synonyms: 1H-Indene-5-carboxylic acid, 2,3-dihydro-2-(3-hydroxy-2-quinolinyl)-1,3-dioxo-, 2-ethoxyethyl ester
• CAS NO: 78333-68-3
• Molecular Formula: C23H19 N O6
• Molecular Weight: 0
• Mol File: 78333-68-3.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1H-Indene-5-carboxylic acid, 2,3-dihydro-2-(3-hydroxy-2-quinolinyl)-1,3-dioxo-, 2-ethoxyethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Indene-5-carboxylic acid, 2,3-dihydro-2-(3-hydroxy-2-quinolinyl)-1,3-dioxo-, 2-ethoxyethyl ester(78333-68-3)
• EPA Substance Registry System: 1H-Indene-5-carboxylic acid, 2,3-dihydro-2-(3-hydroxy-2-quinolinyl)-1,3-dioxo-, 2-ethoxyethyl ester(78333-68-3)

Safety Data

• Hazardous Substances Data: 78333-68-3(Hazardous Substances Data)

Usage

Indene ring

A bicyclic aromatic compound consisting of a six-membered benzene ring fused to a five-membered ring.

Carboxylic acid group

A functional group with a carboxyl (-COOH) moiety attached at the 5th position of the indene ring, contributing to the compound's acidity and potential reactivity.

2,3-Dihydro

The compound has two hydrogen atoms in the 2,3 positions, indicating a reduced ring structure compared to the parent compound.

2-(3-Hydroxy-2-quinolinyl)

A 2-quinoline ring with a hydroxyl (-OH) group at the 3rd position, which is attached to the 2nd position of the dihydro structure, contributing to the compound's polarity and hydrogen bonding potential.

1,3-Dioxo

The compound contains a 1,3-dioxo group, which is a two carbonyl (C=O) functional group separated by an oxygen atom. This group is present in the 2-(3-hydroxy-2-quinolinyl) moiety, increasing the compound's reactivity and potential for forming coordination complexes.

2-Ethoxyethyl ester

An ester functional group (-COO-) attached to an ethoxy (-OCH2CH3) group at the 2nd position of the 1,3-dioxo group. This group contributes to the compound's polarity and may be involved in hydrogen bonding and solubility properties.
These properties and functional groups make the compound potentially useful in pharmaceutical or industrial applications due to its unique structure and reactivity.