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perinone

Structure via PubChem · Public domain (PubChem)

EntityQ2070998· pop 6· linked from 2 articles

Also known as Vat Orange 7, C.I. 71105, C.I. Pigment Orange 43, Bisbenzimidazo[2,1-b:2',1'-i]benzo[lmn][3,8]phenanthroline-8,17-dione

Perinone is a class of organic compounds. The parent compound has two isomers, each of which are useful pigments.

Chemical data

Formula
C26H12N4O2
Molecular weight
412.4 g/mol
IUPAC name
3,10,17,24-tetrazaoctacyclo[13.13.2.02,10.04,9.012,29.016,24.018,23.026,30]triaconta-1(29),2,4,6,8,12,14,16,18,20,22,26(30),27-tridecaene-11,25-dione
SMILES
C1=CC=C2C(=C1)N=C3N2C(=O)C4=CC=C5C6=C(C=CC3=C46)C(=O)N7C5=NC8=CC=CC=C87
InChIKey
DGBWPZSGHAXYGK-UHFFFAOYSA-N
XLogP
4.8
Polar surface area
69.8 Ų
H-bond donors
0
H-bond acceptors
4
Formal charge
0

via PubChem

Wikidata facts

Mass
412.096026
Image
PO43 Orange périnone b.jpg
Show 3 more facts
chemical formula
C₂₆H₁₂N₄O₂
canonical SMILES
C1=CC=C2C(=C1)N=C3N2C(=O)C4=CC=C5C6=C(C=CC3=C46)C(=O)N7C5=NC8=CC=CC=C87
Commons category
Perinone
Sources (2)

via Wikidata · CC0

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Encyclopedic overview

1 sections
Contents
  • References

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 are useful pigments. The trans isomer is called Pigment Orange 43 ("PO43", ) and the cis isomer is called Pigment Red 194 ("PR194", ). Like some structurally related compounds perinone is also an organic semiconductor.

Excerpted from Wikipedia’s “perinone” article, available under the CC BY-SA 4.0 licence.

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