Intermediate of API

2420-87-3

  • Product Name:3,3',4,4'-Biphenyltetracarboxylic dianhydride (BPDA)
  • Molecular Formula:C16H6O6
  • Specifications:99%
  • Molecular Weight:294.22
Inquiry

Product Details;

CasNo: 2420-87-3

Molecular Formula: C16H6O6

Pharmaceutical Grade 99% Purity 3,3',4,4'-Biphenyltetracarboxylic dianhydride (BPDA) 2420-87-3 White Powder

  • Molecular Formula:C16H6O6
  • Molecular Weight:294.22
  • Vapor Pressure:0Pa at 20℃ 
  • Melting Point:299-305 °C 
  • Boiling Point:614.9 °C at 760 mmHg 
  • Flash Point:277.4 °C 
  • PSA:86.74000 
  • Density:1.625 g/cm3 
  • LogP:1.97480 

3,3',4,4'-Biphenyltetracarboxylic dianhydride(Cas 2420-87-3) Usage

Chemical Properties

Off-white solid

Uses

3,3',4,4'-biphenyltetracarboxylic dianhydride be used for the preparation of a polyimide material. This compound has been studied for its potential use in various applications such as in the field of organic electronics, as well as in medicinal chemistry for its potential therapeutic properties.

Preparation

The preparation of 3,3',4,4'-Biphenyltetracarboxylic dianhydride is as follows:In a nitrogen atmosphere, add N-(3-N,N-dimethylamino-propyl)-4-chlorophthalimide (26.65g, 0.1moL),Zinc powder (3.25g, 0.05moL), anhydrous NiCl2 (127.5mg, 1mmoL),Triphenylphosphine (250mg, 1mmoL) and 70 mL of anhydrous DMAc were stirred at 50°C for 24 hours, and 55mL of solvent DMAc was recovered under reduced pressure. Add 80g of xylene to the system and reflux (recrystallize), filter out the inorganic matter, the clarified filtrate will be cooled and precipitated, filtered, and vacuum dried for 10 hours. 21.8g of 3,3',4,4'-biphenylbisimine was obtained with a yield of 94%. In a 100mL reaction flask, add 4.62g (0.01mol) of the above 3,3',4,4'-biphenylbisimine and 9g of 20% sodium hydroxide aqueous solution, and heat to reflux for 24 hours. Filter and adjust pH=1 with concentrated hydrochloric acid to obtain 3,3’,4,4’-biphenyltetracarboxylic acid. After filtering, wash with water three times and reflux with water with 20mL trimethylbenzene.2.85g of white 3,3′,4,4′-biphenyltetracarboxylic dianhydride was obtained, the yield was 97%.

General Description

3,3',4,4'-Biphenyltetracarboxylic dianhydride (BPDA) is a chemical compound that belongs to the class of benzofuran derivatives.

Flammability and Explosibility

Nonflammable

IUPAC Name: 5-(1,3-dioxo-2-benzofuran-5-yl)-2-benzofuran-1,3-dione  
Isomeric SMILES: C1=CC2=C(C=C1C3=CC4=C(C=C3)C(=O)OC4=O)C(=O)OC2=O  
InChIKey: WKDNYTOXBCRNPV-UHFFFAOYSA-N  
InChI: InChI=1S/C16H6O6/c17-13-9-3-1-7(5-11(9)15(19)21-13)8-2-4-10-12(6-8)16(20)22-14(10)18/h1-6H  

2420-87-3 Relevant articles

Method for preparing biphenyldianhydride through microwave-assisted catalytic coupling

-

Paragraph 0027; 0029; 0033; 0035, (2021/11/06)

The invention discloses a method for pre...

Method for preparing and separating and purifying biphenyl derivatives through catalytic coupling

-

Paragraph 0009; 0026; 0029; 0031; 0033; 0034; 0037, (2021/10/11)

The invention discloses a method for pre...

Synthesis and characterization of a novel polyimide derived from 3,3',4,4'-biphenyltetracarboxylic dianhydride and 4,4'-diaminodiphenyl ether for high-performance applications.

Liu, Y., Li, Y., & Li, X.

Polymer Composites, 36(6), 1058-1065.

The article describes the synthesis and characterization of a novel polyimide derived from 3,3',4,4'-biphenyltetracarboxylic dianhydride (BPDA) and 4,4'-diaminodiphenyl ether (ODA) for high-performance applications. The authors synthesized the polyimide by a two-step process involving the preparation of BPDA dianhydride and the subsequent reaction with ODA in a solvent under reflux. 

Method for preparing biphenyldianhydride isomer by ultrasonic-assisted catalytic coupling

-

Paragraph 0024; 0026; 0028; 0030; 0032; 0034, (2021/11/06)

The invention discloses a method for pre...

2420-87-3 Process route

methanol
67-56-1

methanol

benzene-1,2-dicarboxylic acid
88-99-3,73607-73-5

benzene-1,2-dicarboxylic acid

2,3',3,4'-biphenyltetracarboxylic acid dianhydride
36978-41-3

2,3',3,4'-biphenyltetracarboxylic acid dianhydride

2,3,2',3'-biphenyltetracarboxylic dianhydride
3711-04-4

2,3,2',3'-biphenyltetracarboxylic dianhydride

3,3',4,4'-biphenyltetracarboxylic anhydride
2420-87-3

3,3',4,4'-biphenyltetracarboxylic anhydride

Conditions
Conditions Yield
benzene-1,2-dicarboxylic acid; With chlorine; In water; for 3h;
methanol; for 1.5h; Further stages;
 
2,3',3,4'-biphenyltetracarboxylic acid dianhydride
36978-41-3

2,3',3,4'-biphenyltetracarboxylic acid dianhydride

3,3',4,4'-biphenyltetracarboxylic anhydride
2420-87-3

3,3',4,4'-biphenyltetracarboxylic anhydride

Conditions
Conditions Yield
 
 

2420-87-3 Upstream products

  • 22803-05-0
    22803-05-0

    4,4'-biphthalic acid

  • 4342-61-4
    4342-61-4

    1,2-dichlorotetramethylsilane

  • 1204-28-0
    1204-28-0

    trimellitic anhydride acid chloride

  • 4920-95-0
    4920-95-0

    3,4,3',4'-Tetramethylbiphenyl

2420-87-3 Downstream products

  • 14074-63-6
    14074-63-6

    3,3’,4,4’-biphenyltetracarboxylic diimide

  • 1082747-84-9
    1082747-84-9

    2,2'-bis-{6-[ethyl-(2-methoxybenzyl)amino]hexyl}-[5,5']biisoindolyl-1,3,1',3'-tetraone

  • 1509941-64-3
    1509941-64-3

    C25H20N2*C16H10O8

  • 1610847-15-8
    1610847-15-8

    C32H20N2O8