5816-02-4

Basic information

• Product Name: 10,10'-(1,2-ethanediylidene)bisanthracen-9(10H)-one
• Synonyms: 10,10'-(1,2-ethanediylidene)bisanthracen-9(10H)-one
• CAS NO: 5816-02-4
• Molecular Formula: C₃₀H₁₈O₂
• Molecular Weight: 410.46272
• EINECS: 227-387-0
• Mol File: 5816-02-4.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 669.2°Cat760mmHg
• Flash Point: 239.5°C
• Appearance: /
• Density: 1.377g/cm³
• CAS DataBase Reference: 10,10'-(1,2-ethanediylidene)bisanthracen-9(10H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: 10,10'-(1,2-ethanediylidene)bisanthracen-9(10H)-one(5816-02-4)
• EPA Substance Registry System: 10,10'-(1,2-ethanediylidene)bisanthracen-9(10H)-one(5816-02-4)

Safety Data

• Hazardous Substances Data: 5816-02-4(Hazardous Substances Data)

Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule of the compound.

Explanation

It is derived from anthracene, which is a polycyclic aromatic hydrocarbon consisting of three fused benzene rings.

Explanation

The compound appears as a yellow-colored powder at room temperature.

Explanation

The compound dissolves easily in organic solvents, such as alcohols, ethers, and hydrocarbons.

Explanation

It is used as a building block for organic synthesis in various industries, including the production of dyes, pharmaceuticals, and as a reagent in chemical processes.

Explanation

The compound is known for its high purity, which is essential for its use in various applications.

Explanation

It is stable under normal conditions, making it suitable for use in a wide range of industrial and research applications.

Explanation

Due to its high purity and stability, the compound is used in various industrial and research applications, including the synthesis of complex organic molecules and the development of new materials.

Explanation

The chemical structure refers to the specific arrangement of atoms and bonds in the molecule, which determines its properties and reactivity.

Explanation

The compound serves as a building block for the synthesis of more complex organic molecules, making it a valuable tool in the field of organic chemistry.

Derivative of anthracene

Yes

Physical state

Yellow powder

Solubility

Soluble in organic solvents

Applications

Dye intermediates, pharmaceutical intermediates, and chemical reagent

Purity

High purity

Stability

Stable

Industrial and research applications

Wide range

Chemical structure

10,10'-(1,2-ethanediylidene)bisanthracen-9(10H)-one

Building block for organic synthesis

Yes

Upstream product

• 302-17-0 chloral hydrate 
• 90-44-8 anthracen-9(10H)-one 
• 496-45-7 glyoxal sulfate 
• 515-82-2 chloralformamide 
• 64-19-7 acetic acid 
• 75-87-6 chloral 
• 4159-04-0 10-Methylene-10H-anthracen-9-one 
• 58382-05-1 1,2-Di-(9,10-dihydro-9-hydroxy-10-oxoanthryl)-ethan 
• 58382-08-4 10,10'-(Ethane-1,2-diyl)bis(anthracen-9-ol) 
• 72423-87-1 10-bromo-10-(bromomethyl)anthrone 

Downstream Products

• 129-68-0 aceanthryleno[2,1-a]aceanthrylene-5,13-dione 

Relevant articles and documents

Thermal Dimerization of 10-Methyleneanthrone

The thermal reaction of the title compound (1) gave three dimeric products which were formed via a path involving two competitive reactions, Diels-Alder and radical dimerization.