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2421-28-5

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2421-28-5 Usage

Description

Benzophenone-3,3',4, 4'-tetracarboxylic dianhydride (BTDA) is used as intermediate and in polycondensation (fiber and powder production) to manufacture plastic products or fine chemicals in the industrial sector. Consumer risk is very unlikely as BTDA is manufactured and handled under closed conditions in industrial settings only. The environmental effects, ecotoxicology and toxicology information available for BTDA is provided based on studies and/or a reliable evaluation of its hazardous properties.

Uses

Different sources of media describe the Uses of 2421-28-5 differently. You can refer to the following data:
1. BTDA is used as intermediate in the manufacture of plastic products or fine chemicals in the industrial sector.
2. BTDA is important monomer of polyimide, and used for production of polyimide material.
3. Used in the synthesis of polyimides.
4. BTDA polymer fine free-flowing powder suitable for general purposes. BTDA Microfine Micronized powder facilitates mixing in epoxy resins. BTDA ultrapure high-purity, high-assay powder for critical polyimide synthesis.

Physical properties

BTDA is a tan-colored crystalline powder. The substance has a melting point of 218.67 °C and shows decomposition at 360 °C. The auto-ignition temperature is very high and no flammability is observed. The substance has a density of 1.5452 g/ml and a vapor pressure of 6.53E-011 Pa. The substance is slightly water soluble and has a log Pow of 3.3.

Health Hazard

BTDA has no acute toxicity by oral and inhalative route or by dermal exposure. The substance is irritating to eyes and the respiratory tract. BTDA is sensitizing to skin. BTDA is not mutagenic.

Environmental effects

Based on available data for the substance, BTDA is harmful to aquatic organisms with long lasting effects. The substance is not readily biodegradable and is not considered to have potential to bioaccumulate.BTDA is industrially used as monomer to manufacture the rmoplastics or another substance. The manufacture and handling is a closed process, thus only very limited exposure to the environment is expected. Any exposure from manufacture or use will generally be below the level of concern.

Chemical Properties

white crystall powder

General Description

Benzophenone-3,3′,4,4′-tetracarboxylic acid is formed by hydrolysis, it can be converted to the dianhydride by treating with Ac2O (molar ratio 4 to 1 of acid).The dianhydride is used to synthesize polyimides, which are highly flexible in nature due to the presence of keto and carbonyl groups in the dianhydride molecule. The keto and carbonyl groups subsequently increase the spacing between the imide rings enhancing the solubility and processibility.

Flammability and Explosibility

Nonflammable

Purification Methods

The main impurity is the free acid formed by hydrolysis (check for OH bands in the IR). This can be converted to the dianhydride by treating with Ac2O (molar ratio of 4 to 1 of acid), heating at 110-120o for 1.5 to 2hours, cooling to 0—5o and collecting the dianhydride. This is then dissolved in hot dioxane or Me2CO, filtered and cooled to 10—15o. The moisture sensitive solid is collected and dried at 120—130o in vacuo. It has been sublimed at high vacuum. [Faberov et al. J Org Chem USSR 4 153 (English translation) 1968.]

Check Digit Verification of cas no

The CAS Registry Mumber 2421-28-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,2 and 1 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2421-28:
(6*2)+(5*4)+(4*2)+(3*1)+(2*2)+(1*8)=55
55 % 10 = 5
So 2421-28-5 is a valid CAS Registry Number.

2421-28-5 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • TCI America

  • (B0948)  3,3',4,4'-Benzophenonetetracarboxylic Dianhydride  >96.0%(T)

  • 2421-28-5

  • 25g

  • 260.00CNY

  • Detail
  • TCI America

  • (B0948)  3,3',4,4'-Benzophenonetetracarboxylic Dianhydride  >96.0%(T)

  • 2421-28-5

  • 100g

  • 690.00CNY

  • Detail
  • TCI America

  • (B0948)  3,3',4,4'-Benzophenonetetracarboxylic Dianhydride  >96.0%(T)

  • 2421-28-5

  • 500g

  • 2,150.00CNY

  • Detail
  • TCI America

  • (B4260)  3,3',4,4'-Benzophenonetetracarboxylic Dianhydride (purified by sublimation)  >98.0%(GC)

  • 2421-28-5

  • 5g

  • 1,450.00CNY

  • Detail
  • TCI America

  • (B4260)  3,3',4,4'-Benzophenonetetracarboxylic Dianhydride (purified by sublimation)  >98.0%(GC)

  • 2421-28-5

  • 25g

  • 4,990.00CNY

  • Detail
  • Alfa Aesar

  • (A16529)  3,3',4,4'-Benzophenonetetracarboxylic dianhydride, 97+%   

  • 2421-28-5

  • 100g

  • 319.0CNY

  • Detail
  • Alfa Aesar

  • (A16529)  3,3',4,4'-Benzophenonetetracarboxylic dianhydride, 97+%   

  • 2421-28-5

  • 500g

  • 861.0CNY

  • Detail
  • Alfa Aesar

  • (A16529)  3,3',4,4'-Benzophenonetetracarboxylic dianhydride, 97+%   

  • 2421-28-5

  • 2.5kg

  • 2820.0CNY

  • Detail
  • Aldrich

  • (B9750)  Benzophenone-3,3′,4,4′-tetracarboxylicdianhydride  98%

  • 2421-28-5

  • B9750-100G

  • 425.88CNY

  • Detail
  • Aldrich

  • (B9750)  Benzophenone-3,3′,4,4′-tetracarboxylicdianhydride  98%

  • 2421-28-5

  • B9750-500G

  • 1,173.51CNY

  • Detail
  • Aldrich

  • (B9750)  Benzophenone-3,3′,4,4′-tetracarboxylicdianhydride  98%

  • 2421-28-5

  • B9750-5KG

  • 6,552.00CNY

  • Detail

2421-28-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(1,3-dioxo-2-benzofuran-5-carbonyl)-2-benzofuran-1,3-dione

1.2 Other means of identification

Product number -
Other names benzophenone-3,3',4,4'-tetracarboxylic acid dianhydride

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Intermediates
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:2421-28-5 SDS

2421-28-5Synthetic 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
ConditionsYield
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
ConditionsYield
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
View Scheme
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
View Scheme
3,3',4,4'-tetramethyldiphenyldichloromethane

3,3',4,4'-tetramethyldiphenyldichloromethane

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

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

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: sodium hydroxide / water / 1 h / Heating
2: potassium permanganate; water / pyridine / 85 °C
3: diphenylether / 2 h / 230 °C / Dean-Stark; Heating
View Scheme
ethylenediamine
107-15-3

ethylenediamine

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

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

ethane-1,2-diammonium dihydrogen 3,3',4,4'-benzophenonetetracarboxylate

ethane-1,2-diammonium dihydrogen 3,3',4,4'-benzophenonetetracarboxylate

Conditions
ConditionsYield
In water100%
1,3-di(aminomethyl)benzene
1477-55-0

1,3-di(aminomethyl)benzene

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

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

1,3-benzenedimethaneammonium dihydrogen 3,3',4,4'-benzophenonetetracarboxylate

1,3-benzenedimethaneammonium dihydrogen 3,3',4,4'-benzophenonetetracarboxylate

Conditions
ConditionsYield
In water for 0.5h;100%
(naphth-1-yl)methylamine
118-31-0

(naphth-1-yl)methylamine

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

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

4,4'-carbonylbis(2-(naphthalen-1-ylmethylcarbamoyl)benzoic acid)

4,4'-carbonylbis(2-(naphthalen-1-ylmethylcarbamoyl)benzoic acid)

Conditions
ConditionsYield
With triethylamine In tetrahydrofuran at 0℃; for 3h;99%
3,3'-bis(N-aminophthalimide)
916066-54-1

3,3'-bis(N-aminophthalimide)

4,4'-oxydiphenylene diamine
101-80-4

4,4'-oxydiphenylene diamine

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

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

polymer, Mn/Mw = 1.6, Mn = 51210 g/mol, Mw = 82240 g/mol, inherent viscosity = 0.50 dL/g; monomer(s): 3,3\-bis(N-aminophthalimide); 4,4\-oxydianiline; 3,3\44,4\-biphenyltetracarboxylic acid dianhydride

polymer, Mn/Mw = 1.6, Mn = 51210 g/mol, Mw = 82240 g/mol, inherent viscosity = 0.50 dL/g; monomer(s): 3,3\-bis(N-aminophthalimide); 4,4\-oxydianiline; 3,3\44,4\-biphenyltetracarboxylic acid dianhydride

Conditions
ConditionsYield
With 4-chloro-phenol; benzoic acid at 100 - 190℃;98%
[(m-aminophenylamino)-4-aminophenylmethylidene]propanedinitrile
439385-19-0

[(m-aminophenylamino)-4-aminophenylmethylidene]propanedinitrile

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

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

polyimide; monomer(s): [(m-aminophenylamino)-4-aminophenylmethylidene]propanedinitrile; 3,3',4,4'-benzophenone tetracarboxylic dianhydride

polyimide; monomer(s): [(m-aminophenylamino)-4-aminophenylmethylidene]propanedinitrile; 3,3',4,4'-benzophenone tetracarboxylic dianhydride

Conditions
ConditionsYield
In 1-methyl-pyrrolidin-2-one; chlorobenzene at 20 - 190℃; for 20h;98%
1-amino-naphthalene
134-32-7

1-amino-naphthalene

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

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

4,4'-carbonylbis(2-(naphthalen-1-ylcarbamoyl)benzoic acid)

4,4'-carbonylbis(2-(naphthalen-1-ylcarbamoyl)benzoic acid)

Conditions
ConditionsYield
With triethylamine In tetrahydrofuran at 0℃; for 3h;98%
1,1,1,3,3,3-hexamethyl-disilazane
999-97-3

1,1,1,3,3,3-hexamethyl-disilazane

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

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

C23H24N2O5Si2

C23H24N2O5Si2

Conditions
ConditionsYield
at 130 - 140℃;97%
1,4-bis(3-aminopropyl)piperazine
7209-38-3

1,4-bis(3-aminopropyl)piperazine

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

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

polymer, inherent viscosity 0.50 dl/g; monomer(s): bis(3-aminopropyl)piperazine; 3,3\,,4,4\-benzophenonetetracarboxylic dianhydride

polymer, inherent viscosity 0.50 dl/g; monomer(s): bis(3-aminopropyl)piperazine; 3,3\,,4,4\-benzophenonetetracarboxylic dianhydride

Conditions
ConditionsYield
With acetic acid at 130℃; for 12h;94.2%
4-amino-phenol
123-30-8

4-amino-phenol

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

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

N,N′-bis(4-hydroxyphenyl)benzophenone-3,3′,4,4′-tetracarboxylic diimide
53417-18-8

N,N′-bis(4-hydroxyphenyl)benzophenone-3,3′,4,4′-tetracarboxylic diimide

Conditions
ConditionsYield
In N,N-dimethyl-formamide at 20℃; for 12h; Reflux;94%
In N,N-dimethyl-formamide for 5h; Reflux;94%
In N,N-dimethyl-formamide Reflux;
2,5-Dimethyl-1,4-phenylenediamine
6393-01-7

2,5-Dimethyl-1,4-phenylenediamine

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

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

C33H26N4O5

C33H26N4O5

Conditions
ConditionsYield
Stage #1: 2,5-Dimethyl-1,4-phenylenediamine; dianhydride of benzophenone-3,4,3',4'-tetracarboxy acid In 1-methyl-pyrrolidin-2-one at 20℃; for 12h;
Stage #2: In 1-methyl-pyrrolidin-2-one; toluene at 180℃; for 9h; Inert atmosphere;
92.7%
dianhydride of benzophenone-3,4,3',4'-tetracarboxy acid
2421-28-5

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

butan-1-ol
71-36-3

butan-1-ol

3,3',4,4'-benzophenone tetrabutylate

3,3',4,4'-benzophenone tetrabutylate

Conditions
ConditionsYield
With sulfuric acid at 120℃;92.45%
dianhydride of benzophenone-3,4,3',4'-tetracarboxy acid
2421-28-5

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

3-2,2'-(1,2-phenylene)-bis(5-aminobenzimidazole)
313666-93-2

3-2,2'-(1,2-phenylene)-bis(5-aminobenzimidazole)

polymer; monomer(s): 2,2\-(1,2-phenylene)-bis(5-aminobenzimidazole); benzophenone tetracarboxylic dianhydride

polymer; monomer(s): 2,2\-(1,2-phenylene)-bis(5-aminobenzimidazole); benzophenone tetracarboxylic dianhydride

Conditions
ConditionsYield
With 1-methyl-pyrrolidin-2-one In toluene at 140 - 190℃; for 7h;92%
3,3'-bis(N-aminophthalimide)
916066-54-1

3,3'-bis(N-aminophthalimide)

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

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

polymer, Mn/Mw = 1.1, Mn = 21000 g/mol, Mw = 22180 g/mol, inherent viscosity = 0.19 dL/g; monomer(s): 3,3\-bis(N-aminophthalimide); 3,3\44,4\-benzophenonetetracarboxylic acid dianhydride

polymer, Mn/Mw = 1.1, Mn = 21000 g/mol, Mw = 22180 g/mol, inherent viscosity = 0.19 dL/g; monomer(s): 3,3\-bis(N-aminophthalimide); 3,3\44,4\-benzophenonetetracarboxylic acid dianhydride

Conditions
ConditionsYield
With 4-chloro-phenol; benzoic acid at 100 - 190℃;92%
1,4-pyrazine
290-37-9

1,4-pyrazine

cobalt(II) nitrate hexahydrate

cobalt(II) nitrate hexahydrate

water
7732-18-5

water

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

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

[Co2(3,3',4,4'-benzophenone tetracarboxylate)(pyrazine)(H2O)4]*H2O

[Co2(3,3',4,4'-benzophenone tetracarboxylate)(pyrazine)(H2O)4]*H2O

Conditions
ConditionsYield
With Na2CO3 In water High Pressure; under hydrothermal conditions; mixt. of Co salt, Na2CO3, benzophenone dianhydride and pyrazine (molar ratio 2:2:1:2) in H2O introduced into Parrstainless steel vessel; sealed; heated to 160°C for 3 d; cooled (0.5°C/min); crystals collected; elem. anal.;92%
5-Aminouracil
932-52-5

5-Aminouracil

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

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

N,N′-bis(uracil-5-yl)benzophenone-3,3′,4,4′-tetracarboxylic diimide

N,N′-bis(uracil-5-yl)benzophenone-3,3′,4,4′-tetracarboxylic diimide

Conditions
ConditionsYield
In N,N-dimethyl-formamide for 5h; Reflux;91%
glycine
56-40-6

glycine

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

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

[5-(2-Carboxymethyl-1,3-dioxo-2,3-dihydro-1H-isoindole-5-carbonyl)-1,3-dioxo-1,3-dihydro-isoindol-2-yl]-acetic acid
104972-17-0

[5-(2-Carboxymethyl-1,3-dioxo-2,3-dihydro-1H-isoindole-5-carbonyl)-1,3-dioxo-1,3-dihydro-isoindol-2-yl]-acetic acid

Conditions
ConditionsYield
With acetic acid at 120℃; for 7h;90%
ethanol
64-17-5

ethanol

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

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

3,3',4,4'-benzophenonetetracarboxylic acid ethylester
34531-33-4

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

Conditions
ConditionsYield
With sulfuric acid at 150℃;90%
Heating;
meta-aminobenzoic acid
99-05-8

meta-aminobenzoic acid

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

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

C31H16N2O9
105377-29-5

C31H16N2O9

Conditions
ConditionsYield
With acetic acid Reflux;90%
m-Hydroxyaniline
591-27-5

m-Hydroxyaniline

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

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

N,N′-bis(3-hydroxyphenyl)benzophenone-3,3′,4,4′-tetracarboxylic diimide
54942-20-0

N,N′-bis(3-hydroxyphenyl)benzophenone-3,3′,4,4′-tetracarboxylic diimide

Conditions
ConditionsYield
In N,N-dimethyl-formamide for 5h; Reflux;90%
In N,N-dimethyl-formamide Reflux;
propan-1-ol-3-amine
156-87-6

propan-1-ol-3-amine

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

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

N,N′-bis(3-hydroxyprop-1-yl)benzophenone-3,3′,4,4′-tetracarboxylic diimide

N,N′-bis(3-hydroxyprop-1-yl)benzophenone-3,3′,4,4′-tetracarboxylic diimide

Conditions
ConditionsYield
In N,N-dimethyl-formamide for 5h; Reflux;90%
S-trityl-L-cysteine
2799-07-7

S-trityl-L-cysteine

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

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

C61H44N2O9S2

C61H44N2O9S2

Conditions
ConditionsYield
With dmap In N,N-dimethyl-formamide at 140℃; for 0.166667h; Sealed tube; Microwave irradiation;90%
ethanolamine
141-43-5

ethanolamine

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

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

N,N′-bis(2-hydroxyethyl)benzophenone-3,3′,4,4′-tetracarboxylic diimide

N,N′-bis(2-hydroxyethyl)benzophenone-3,3′,4,4′-tetracarboxylic diimide

Conditions
ConditionsYield
In N,N-dimethyl-formamide for 5h; Reflux;89%
2-amino-phenol
95-55-6

2-amino-phenol

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

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

N,N′-bis(2-hydroxyphenyl)benzophenone-3,3′,4,4′-tetracarboxylic diimide

N,N′-bis(2-hydroxyphenyl)benzophenone-3,3′,4,4′-tetracarboxylic diimide

Conditions
ConditionsYield
In N,N-dimethyl-formamide for 5h; Reflux;89%
(Benzocyclobutenyl)methylamine
1005-19-2

(Benzocyclobutenyl)methylamine

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

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

C35H24N2O5

C35H24N2O5

Conditions
ConditionsYield
Stage #1: (Benzocyclobutenyl)methylamine; dianhydride of benzophenone-3,4,3',4'-tetracarboxy acid In N,N-dimethyl-formamide at 20℃; for 6h; Inert atmosphere;
Stage #2: With tributyl-amine; acetic anhydride In N,N-dimethyl-formamide at 100℃; for 4h; Inert atmosphere;
89%
L-valine
72-18-4

L-valine

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

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

(S)-2-{5-[2-((S)-1-Carboxy-2-methyl-propyl)-1,3-dioxo-2,3-dihydro-1H-isoindole-5-carbonyl]-1,3-dioxo-1,3-dihydro-isoindol-2-yl}-3-methyl-butyric acid
141523-60-6

(S)-2-{5-[2-((S)-1-Carboxy-2-methyl-propyl)-1,3-dioxo-2,3-dihydro-1H-isoindole-5-carbonyl]-1,3-dioxo-1,3-dihydro-isoindol-2-yl}-3-methyl-butyric acid

Conditions
ConditionsYield
With acetic acid at 20℃; for 12.5h; Reflux;85.6%
With acetic acid at 120℃; for 7h;84%
dianhydride of benzophenone-3,4,3',4'-tetracarboxy acid
2421-28-5

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

3-amino propanoic acid
107-95-9

3-amino propanoic acid

3-{5-[2-(2-Carboxy-ethyl)-1,3-dioxo-2,3-dihydro-1H-isoindole-5-carbonyl]-1,3-dioxo-1,3-dihydro-isoindol-2-yl}-propionic acid
128007-92-1

3-{5-[2-(2-Carboxy-ethyl)-1,3-dioxo-2,3-dihydro-1H-isoindole-5-carbonyl]-1,3-dioxo-1,3-dihydro-isoindol-2-yl}-propionic acid

Conditions
ConditionsYield
With acetic acid at 120℃; for 7h;84%
dianhydride of benzophenone-3,4,3',4'-tetracarboxy acid
2421-28-5

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

3,3',4,4'-benzophenonetetracarboxylic acid diimide
6097-10-5

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

Conditions
ConditionsYield
With formamide for 0.0416667h; microwave irradiation;84%
With urea In N,N-dimethyl-formamide at 110℃; for 3h;
L-leucine
61-90-5

L-leucine

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

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

(S)-2-{5-[2-((S)-1-Carboxy-3-methyl-butyl)-1,3-dioxo-2,3-dihydro-1H-isoindole-5-carbonyl]-1,3-dioxo-1,3-dihydro-isoindol-2-yl}-4-methyl-pentanoic acid
141523-61-7

(S)-2-{5-[2-((S)-1-Carboxy-3-methyl-butyl)-1,3-dioxo-2,3-dihydro-1H-isoindole-5-carbonyl]-1,3-dioxo-1,3-dihydro-isoindol-2-yl}-4-methyl-pentanoic acid

Conditions
ConditionsYield
With acetic acid at 120℃; for 7h;80%

2421-28-5Relevant articles and documents

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 experiments conducted in order to develop a laboratory method for producing 3,3′, 4,4′-benzophenonetetracarboxylic dianhydride and selection of the optimum conditions, allowing to obtain the greatest yield. 3,3′, 4,4′-benzophenonetetracarboxylic dianhydride is used for the preparation of polyimides with high thermal stability, chemical resistance as well as high strength and high Young's modulus. Benzophenonetetracarboxylic dianhydride was prepared by multistep route: Friedel-Crafts alkylation of o-xylene to obtain 3,3′, 4,4′-tetramethyl benzophenone followed by liquid phase oxidation to benzophenonetetracarboxylic acid and dehydration.

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 catalysis for the dehydrative self-condensation of carboxylic acids is described. Arylboronic acid bearing bulky (N,N-dialkylamino)methyl groups at the 2,6-positions can catalyze the intramolecular dehydrative condensation of di-and tetracarboxylic acids. This is the first successful method for the catalytic dehydrative self-condensation of carboxylic acids.(Figure Presented)

Inkjet ink

-

, (2008/06/13)

The invention relates to a method for manufacturing an inkjet ink including a polyamic acid (A), including a step of at least reacting one or more compounds selected from the group of a monoamine (a3) and a compound having one acid anhydride group (a4) with a compound having two or more acid anhydride groups (a1) and a diamine (a2).

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