- CasNo 5690-24-4
- Purity 99%
Location:Home > Organic Chemicals
1,4,5,8-NAPHTHALENETETRACARBOXDIIMIDE 5690-24-4 with purity >99% Low price in stock
- Molecular Formula: C14H6 N2 O4
- Molecular Weight: 266.213
- Vapor Pressure: 1.33E-19mmHg at 25°C
- Melting Point: >410 °C
- Boiling Point: 702.8°Cat760mmHg
- PKA: 7.98±0.20(Predicted)
- Flash Point: 311.1°C
- PSA： 99.86000
- Density: 1.666g/cm3
- LogP: 0.11880
1,4,5,8-NAPHTHALENETETRACARBOXDIIMIDE(Cas 5690-24-4) Usage
|
General Description |
1,4,5,8-Naphthalenetetracarboxdiimide is a chemical compound with the molecular formula C14H4N2O6. It is a synthetic organic compound that is commonly used as a blue pigment in dyes and inks. 1,4,5,8-Naphthalenetetracarboxdiimide is also used as a precursor in the production of other chemicals and materials. It has been studied for its potential applications in organic semiconductors and as a building block for the synthesis of complex organic molecules. However, it is important to handle this chemical with care, as it is classified as a hazardous substance and should be used in accordance with safety guidelines and regulations. |
InChI:InChI=1/C14H6N2O4/c17-11-5-1-2-6-10-8(14(20)16-12(6)18)4-3-7(9(5)10)13(19)15-11/h1-4H,(H,15,17,19)(H,16,18,20)
5690-24-4 Relevant articles
A facile synthesis of 2,7-diazapyrene
Sotiriou-Leventis,Mao
, p. 1665 - 1667 (2000)
2,7-Diazapyrene is synthesized in three ...
Synthesis and crystal packing structures of 2,7-diazapyrenes with various alkyl groups at 1,3,6,8-positions
Matsuda, Wakana,Miyake, Yoshihiro,Nakazato, Takumi,Sakurai, Tsuneaki,Seki, Shu,Shinokubo, Hiroshi
, p. 465 - 468 (2020)
We have developed the synthesis of 1,3,6...
Molecular Orientation Change in Naphthalene Diimide Thin Films Induced by Removal of Thermally Cleavable Substituents
Nakamura, Tomoya,Shioya, Nobutaka,Shimoaka, Takafumi,Nishikubo, Ryosuke,Hasegawa, Takeshi,Saeki, Akinori,Murata, Yasujiro,Murdey, Richard,Wakamiya, Atsushi
, p. 1729 - 1737 (2019)
The potential of naphthalene-1,8:4,5-tet...
Macrocyclization and molecular interlocking via Mitsunobu alkylation: Highlighting the role of C-H...O interactions in templating
Hansen, Jimmi G.,Feeder, Neil,Hamilton, Darren G.,Gunter, Maxwell J.,Becher, Jan,Sanders, Jeremy K. M.
, p. 449 - 452 (2000)
(Formula presented) A series of diimide-...
The reductive aromatization of naphthalene diimide: A versatile platform for 2,7-diazapyrenes
Nakazato, Takumi,Kamatsuka, Takuto,Inoue, Junichi,Sakurai, Tsuneaki,Seki, Shu,Shinokubo, Hiroshi,Miyake, Yoshihiro
, p. 5177 - 5180 (2018)
The reductive aromatization of naphthale...
Effects of Zn2+and H+association with naphthalene diimide electrodes for aqueous Zn-ion batteries
Byon, Hye Ryung,Na, Moony,Oh, Yusik
, p. 6990 - 6997 (2020)
Organic electrodes have been extensively...
5690-24-4 Process route
-
-
81-30-1
1,4,5,8-naphthalenetetracarboxylic dianhydride
-
-
5690-24-4
1,4,5,8-naphthalenetetracaraboxylic dianhydride
Conditions
| Conditions | Yield |
|---|---|
|
With
ammonium hydroxide;
at 20 ℃;
for 6h;
|
96%
|
|
With
formamide;
for 0.0833333h;
microwave irradiation;
|
96%
|
|
With
ammonium hydroxide;
In
water;
at 20 ℃;
|
96%
|
|
With
ammonium acetate;
In
acetic acid;
for 1h;
Reflux;
|
95%
|
|
With
formamide;
In
neat (no solvent);
for 0.333333h;
Reagent/catalyst;
Milling;
Heating;
Green chemistry;
|
94%
|
|
With
ammonium hydroxide;
In
water;
at 60 ℃;
for 1h;
|
89%
|
|
With
ammonium hydroxide;
at 20 ℃;
for 24h;
Inert atmosphere;
|
87%
|
|
With
ammonium hydroxide;
at 20 ℃;
for 24h;
Inert atmosphere;
|
87%
|
|
With
ammonium hydroxide;
at 20 ℃;
for 8h;
|
86%
|
|
With
formamide;
at 210 ℃;
for 0.25h;
Yield given;
|
|
|
With
ammonium hydroxide;
at 20 ℃;
|
|
|
With
ammonium hydroxide;
at 20 ℃;
for 6h;
Inert atmosphere;
|
-
-
5,8-dichloro-naphthalene-1,4-dicarbonitrile
-
-
5690-24-4
1,4,5,8-naphthalenetetracaraboxylic dianhydride
Conditions
| Conditions | Yield |
|---|---|
|
With
potassium cyanide;
at 200 ℃;
|
5690-24-4 Upstream products
-
858436-00-7
4,8-dichloro-naphthalene-1,5-dicarboxylic acid
-
81-30-1
1,4,5,8-naphthalenetetracarboxylic dianhydride
-
7664-41-7
ammonia
-
1825-30-5
1,5-dichloronaphthalene
5690-24-4 Downstream products
-
910138-52-2
(R)-2-[7-((R)-1-carboxy-2-tritylsulfanyl-ethyl)-1,3,6,8-tetraoxo-3,6,7,8-tetrahydro-1H-benzo[lmn][3,8]phenanthrolin-2-yl]-3-tritylsulfanyl-propionic acid
-
1246286-32-7
(((1,3,6,8-tetraoxobenzo[lmn][3,8]phenanthroline-2,7(1H,3H,6H,8H)-diyl)bis(ethane-2,1-diyl))bis(oxy))bis(ethane-2,1-diyl)bis(4-methylbenzenesulfonate)
-
34151-51-4
N,N’-bis(4-pyridylmethyl)-1,4,5,8-naphthalenetetra-carboxydiimide
-
828301-12-8
[S,S]-N,N'-bis-[4-(benzyloxycarbonyl)-2-(N-5-fluoro-2,4-dinitrophenylamino)-butanoyl]-2,7-diaza-1,2,3,6,7,8-hexahydropyrene
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