Benzanthrone

Base Information

  • Chemical Name: Benzanthrone
  • CAS No.: 82-05-3

Factory Sells Best Quality Benzanthrone 82-05-3 with steady supply

  • Molecular Formula: C17H10O
  • Molecular Weight: 230.266
  • Appearance/Colour: Light yellow powder 
  • Vapor Pressure: 8.27E-08mmHg at 25°C 
  • Melting Point: 170 °C 
  • Refractive Index: 1.734 
  • Boiling Point: 436.2 °C at 760 mmHg 
  • Flash Point: 196.1 °C 
  • PSA: 17.07000 
  • Density: 1.286 g/cm3 
  • LogP: 4.05120 

Benzanthrone(Cas 82-05-3) Usage

Reactivity Profile

Benzanthrone is incompatible with nitrobenzene and potassium hydroxide. Benzanthrone is also incompatible with strong oxidizing agents.

Fire Hazard

Flash point data for Benzanthrone are not available; however, Benzanthrone is probably combustible.

Purification Methods

Crystallise benzanthrone from EtOH or xylene. [Beilstein 7 IV 1819.]

Definition

A four-ring system.

InChI:InChI=1/C17H10O/c18-17-14-8-2-1-7-12(14)13-9-3-5-11-6-4-10-15(17)16(11)13/h1-10H

82-05-3 Relevant articles

Synthesis and Characterization of Polysubstituted Dibenzopyrenes as Charge-Transporting Materials

Kumar, Sushil,Ho, Man-Tzu,Tao, Yu-Tai

, p. 4876 - 4879 (2016)

A new class of benzopyrene-based semicon...

Novel production method of phenanthrone (by machine translation)

-

Paragraph 0031-0043, (2020/01/25)

The invention relates to the field of, f...

Compound with anthrene structure and application of compound in organic light emitting diode devices

-

Paragraph 0065-0067; 0078, (2020/03/16)

The invention discloses a compound with ...

Benzanthrone derivative and preparation method thereof and application thereof in functional pigments

-

, (2020/07/24)

The invention discloses a benzanthrone d...

Palladium-Catalyzed Site-Selective Benzocyclization of Naphthoic Acids with Diaryliodonium Salts: Efficient Access to Benzanthrones

Xue, Chenwei,Wang, Limin,Han, Jianwei

, p. 15406 - 15414 (2020/12/23)

Dual activation of both C-I and vicinal ...

82-05-3 Process route

1-benzoylnaphthalene
642-29-5

1-benzoylnaphthalene

naphthalene
91-20-3,71998-51-1,72931-45-4

naphthalene

7H-benz[d,e]anthracene-7-one
82-05-3

7H-benz[d,e]anthracene-7-one

C<sub>6</sub>H<sub>5</sub>COC<sub>10</sub>H<sub>7</sub>
644-13-3

C6 H5 COC10 H7

Conditions
Conditions Yield
With polyphosphoric acid; at 160 ℃; for 6h; Temperature; Inert atmosphere;
56%
8%
5%
benzoyl chloride
98-88-4

benzoyl chloride

7H-benz[d,e]anthracene-7-one
82-05-3

7H-benz[d,e]anthracene-7-one

C<sub>6</sub>H<sub>5</sub>COC<sub>10</sub>H<sub>7</sub>
644-13-3

C6 H5 COC10 H7

Conditions
Conditions Yield
Multi-step reaction with 2 steps
1: aluminum (III) chloride / dichloromethane / 0 °C
2: polyphosphoric acid / 6 h / 160 °C / Inert atmosphere
With aluminum (III) chloride; In dichloromethane; 1: |Friedel-Crafts Acylation;

82-05-3 Upstream products

  • 107-94-8
    107-94-8

    chloropropionic acid

  • 4159-04-0
    4159-04-0

    10-Methylene-10H-anthracen-9-one

  • 85-44-9
    85-44-9

    phthalic anhydride

  • 642-29-5
    642-29-5

    1-benzoylnaphthalene

82-05-3 Downstream products

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    119-91-5

    2,2'-biquinoline

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    128-64-3

    isoviolanthrone

  • 191-53-7
    191-53-7

    4,5:11,12-dibenzoperopyren

  • 116-90-5
    116-90-5

    4,4'-dibenzanthronyl

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