2421-28-5

  • Product Name:3,3',4,4'-Diphenylketone Tetracarboxylic Acid Dianhydride
  • MF:C17H6O7
  • Purity:99%
  • Molecular Weight:322.23
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Product Details

3,3',4,4'-Diphenylketone Tetracarboxylic Acid Dianhydride 2421-28-5 with purity >99% Low price in stock

  • Molecular Formula:C17H6O7
  • Molecular Weight:322.23
  • Appearance/Colour:white crystal powder 
  • Vapor Pressure:<0.1 mm Hg ( 0 °C) 
  • Melting Point:218-222 °C(lit.) 
  • Refractive Index:1.6380 (estimate) 
  • Boiling Point:638.8 °C at 760 mmHg 
  • Flash Point:286.1 °C 
  • PSA:103.81000 
  • Density:1.662 g/cm3 
  • LogP:1.53880 

2421-28-5 Relevant articles

Development and optimization of producing 3,3′, 4,4′-benzophenonetetracarboxylic dianhydride

Yegorov, Anton Sergeyevich,Wozniak, Alyona Igorevna,Ivanov, Vitaly Sergeyevich,Averina, Elena Aleksandrovna,Zhdanovich, Olga Anatolevna

, p. 3063 - 3070 (2016)

This paper includes a series of experime...

A 3,3 the [...], 4,4 the method for preparing [...] -benzophenone tetracidic dianhydride

-

Paragraph 0024-0027, (2017/02/09)

The invention discloses a method for syn...

Bronsted base-assisted boronic acid catalysis for the dehydrative intramolecular condensation of dicarboxylic acids

Sakakura, Akira,Ohkubo, Takuro,Yamashita, Risa,Akakura, Matsujiro,Ishihara, Kazuaki

supporting information; experimental part, p. 892 - 895 (2011/05/02)

Bronsted base-assisted boronic acid cata...

METHOD FOR PRODUCING CARBOXYLIC ANHYDRIDE AND ARYLBORONIC ACID COMPOUND

-

Page/Page column 10-11, (2012/01/13)

When phthalic acid is heated in heptane ...

2421-28-5 Process route

3,3',4,4'-benzophenonetetracarboxylic acid
2479-49-4

3,3',4,4'-benzophenonetetracarboxylic acid

dianhydride of benzophenone-3,4,3',4'-tetracarboxy acid
2421-28-5

dianhydride of benzophenone-3,4,3',4'-tetracarboxy acid

Conditions
Conditions Yield
With 2,6-bis[(2,2,6,6-tetramethylpiperidin-1-yl)methyl]phenylboronic acid; In propyl cyanide; for 12h; Reflux;
98%
at 225 ℃; for 2h; Industrial scale;
73.56%
In diphenylether; at 230 ℃; for 2h; Dean-Stark; Heating;
70%
o-xylene
95-47-6

o-xylene

dianhydride of benzophenone-3,4,3',4'-tetracarboxy acid
2421-28-5

dianhydride of benzophenone-3,4,3',4'-tetracarboxy acid

Conditions
Conditions Yield
Multi-step reaction with 3 steps
1.1: 3 h / 0 - 2 °C / Inert atmosphere; Industrial scale
1.2: 7 h / 0 - 40 °C / Inert atmosphere; Industrial scale
2.1: potassium permanganate; hydrogenchloride / water / 3 h / 80 °C / Industrial scale
3.1: 2 h / 225 °C / Industrial scale
With hydrogenchloride; potassium permanganate; In water;
Multi-step reaction with 4 steps
1: aluminum (III) chloride / 0 - 5 °C
2: sodium hydroxide / water / 1 h / Heating
3: potassium permanganate; water / pyridine / 85 °C
4: diphenylether / 2 h / 230 °C / Dean-Stark; Heating
With aluminum (III) chloride; potassium permanganate; water; sodium hydroxide; In pyridine; diphenylether; water; 1: |Friedel-Crafts Alkylation;

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