124190-19-8

Basic information

• Product Name: 2,4,9-trihydroxy-6-methoxy-7-methyl-2-(2-oxopropyl)-1H-phenalene-1,3(2H)-dione
• Synonyms: (-)-2,4,9-Trihydroxy-6-methoxy-7-methyl-2-(2-oxopropyl)-1H-phenalene-1,3(2H)-dione; 1H-phenalene-1,3(2H)-dione, 2,4,9-trihydroxy-6-methoxy-7-methyl-2-(2-oxopropyl)-, (-)-; 2-Acetonyl-2,4,9-trihydroxy-6-methoxy-7-methyl-1H-phenalene-1,3(2H)-dione
• CAS NO: 124190-19-8
• Molecular Formula: C₁₈H₁₆O₇
• Molecular Weight: 344.3154
• Mol File: 124190-19-8.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 681.8°C at 760 mmHg
• Flash Point: 252.6°C
• Density: 1.501g/cm³
• Vapor Pressure: 1.6E-19mmHg at 25°C
• Refractive Index: 1.686
• CAS DataBase Reference: 2,4,9-trihydroxy-6-methoxy-7-methyl-2-(2-oxopropyl)-1H-phenalene-1,3(2H)-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4,9-trihydroxy-6-methoxy-7-methyl-2-(2-oxopropyl)-1H-phenalene-1,3(2H)-dione(124190-19-8)
• EPA Substance Registry System: 2,4,9-trihydroxy-6-methoxy-7-methyl-2-(2-oxopropyl)-1H-phenalene-1,3(2H)-dione(124190-19-8)

Safety Data

• Hazardous Substances Data: 124190-19-8(Hazardous Substances Data)

Usage

Explanation

The compound consists of 18 carbon atoms, 18 hydrogen atoms, and 8 oxygen atoms.

Explanation

The total mass of one mole of the compound, calculated from the molecular formula.

Explanation

The compound's structure is characterized by these functional groups, which contribute to its chemical properties and potential applications.

Explanation

The core structure of the compound is based on the phenalene-1,3(2H)-dione backbone, which provides a foundation for the attachment of the functional groups.

Explanation

A propyl-oxo side chain is attached to the main structure, which may influence the compound's solubility, reactivity, and other properties.

Explanation

The compound may have potential uses in the pharmaceutical industry due to its structural features, such as antioxidant, anti-inflammatory, or antimicrobial properties.

Explanation

While the compound has potential applications, further research and testing are required to determine its specific properties and suitability for use in various industries.

Molecular weight

374.33 g/mol

Chemical structure

Three hydroxyl groups, a methoxy group, a methyl group, and two carbonyl groups

Derived from

Phenalene-1,3(2H)-dione backbone

Propyl-oxo side chain

2-(2-oxopropyl)

Potential applications

Pharmaceuticals

Further research needed

Specific properties and potential uses in medicine, agriculture, or materials science

Upstream product

• 67-64-1 acetone 

Relevant articles and documents

Total Syntheses of FR-901235, Auxarthrones A-D, and Lamellicolic Anhydride

In our previous study, an unusual rearrangement reaction was discovered whereby dinaphthyl ketones with three hydroxy groups at restricted positions were transformed into a phenalenone ring and a benzene ring. Using the rearrangement as a key reaction, the first total syntheses of FR-901235 and auxarthrones A-D from an unstable triketone common intermediate are described. Furthermore, lamellicolic anhydride was synthesized from the triketone. This conversion is part of the putative biosynthetic pathway and was achieved experimentally for the first time.