Identifiers | |
---|---|
3D model (
JSmol)
|
|
ChemSpider | |
ECHA InfoCard | 100.022.363 |
EC Number |
|
PubChem
CID
|
|
CompTox Dashboard (
EPA)
|
|
| |
| |
Properties | |
C26H12N4O2 | |
Molar mass | 412.408 g·mol−1 |
Appearance | Orange solid |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
Perinone is a class of organic compounds. The parent compound has two isomers, each of which are useful pigments.
It is prepared from naphthalenetetracarboxylic dianhydride by condensation with o-phenylenediamine. The two Isomers of perinone [1] are useful pigments. The trans isomer is called Pigment Orange 43 ("PO43", CID 78141 from PubChem) and the cis isomer is called Pigment Red 194 ("PR194", CID 77892 from PubChem). [2] Like some structurally related compounds perinone is also an organic semiconductor. [3]
Identifiers | |
---|---|
3D model (
JSmol)
|
|
ChemSpider | |
ECHA InfoCard | 100.022.363 |
EC Number |
|
PubChem
CID
|
|
CompTox Dashboard (
EPA)
|
|
| |
| |
Properties | |
C26H12N4O2 | |
Molar mass | 412.408 g·mol−1 |
Appearance | Orange solid |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
Perinone is a class of organic compounds. The parent compound has two isomers, each of which are useful pigments.
It is prepared from naphthalenetetracarboxylic dianhydride by condensation with o-phenylenediamine. The two Isomers of perinone [1] are useful pigments. The trans isomer is called Pigment Orange 43 ("PO43", CID 78141 from PubChem) and the cis isomer is called Pigment Red 194 ("PR194", CID 77892 from PubChem). [2] Like some structurally related compounds perinone is also an organic semiconductor. [3]