605-83-4

Basic information

• Product Name: 9-ethylanthracene
• Synonyms: 9-ethylanthracene
• CAS NO: 605-83-4
• Molecular Formula: C₁₆H₁₄
• Molecular Weight: 206.28
• Mol File: 605-83-4.mol
• Article Data: 3

Chemical Properties

• Melting Point: 60°C
• Boiling Point: 375.14°C (estimate)
• Flash Point: 165.1°C
• Appearance: /
• Density: 1.0413
• Vapor Pressure: 3.57E-05mmHg at 25°C
• Refractive Index: 1.6767
• CAS DataBase Reference: 9-ethylanthracene(CAS DataBase Reference)
• NIST Chemistry Reference: 9-ethylanthracene(605-83-4)
• EPA Substance Registry System: 9-ethylanthracene(605-83-4)

Safety Data

• Hazardous Substances Data: 605-83-4(Hazardous Substances Data)

Usage

InChI:InChI=1/C16H14/c1-2-14-15-9-5-3-7-12(15)11-13-8-4-6-10-16(13)14/h3-11H,2H2,1H3

Upstream product

• 74928-67-9 9-(1-hydroxyethyl)anthracene 
• 28591-87-9 bromo-9 ethyl-10 anthracene 
• 100-67-4 potassium phenolate 
• 166-88-1 9,10-Dihydro-9-spiro 
• 3990-97-4 tert-Butyl β-(9-anthryl)perpropanoate 
• 106778-21-6 8a,9-dihydro-8a-methyl-9-methyleneanthracene 
• 56-23-5 tetrachloromethane 
• 875246-75-6 9-ethyl-1,2,3,4,5,6,7,8-octahydro-anthracene 

Downstream Products

• 2444-68-0 9-vinylanthracene 
• 128842-81-9 9-(α-Bromoethyl)anthracene 
• 96555-83-8 (8b-Benzoyl-4b-ethyl-8b,8d-dihydro-4bH-dibenzo[a,f]cyclopropa[cd]pentalen-8c-yl)-phenyl-methanone 

Relevant articles and documents

The Observation of a Thermal 'Double Aromatization' Process in a Hydrocarbon with Fused Blocked Aromatic Rings

On heating above 150 deg C, compound (1), the first reported example of a hydrocarbon with fused blocked aromatic rings, rearranges to form 9-ethylanthracene, with simultaneous aromatization of two non-aromatic rings.

TELE-SUBSTITUTIONS EN SERIE ANTHRACENIQUE - II; EXTENSION DE LA SUBSTITUTION PAR L'ION PHENATE A DIVERS BROMO-9 ANTHRACENES MESO-ALKYLES

A competition between normal substitution and tele-substitution is observed with 9-bromoanthracenes bearing in the opposite meso position an ethyl, 1b, or a benzyl group 1d.When treated with potassium phenoxide in HMPT these bromides afford mixtures of 9-alkyl-10-phenoxy-anthracenes 2 and 9-α(phenoxyalkyl) anthracenes 3.On the other hand 9-bromo-10 isopropylanthracene 1c is quite unreactive and 9-bromo-10-methoxymethylanthracene 1e leads essentyally to anthraldehyde 7.