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Naphthalenetetracarboxylic dianhydride information


Naphthalenetetracarboxylic dianhydride
NTDA
Names
Preferred IUPAC name
Naphtho[1,8-cd:4,5-cd′]dipyran-1,3,6,8-tetrone
Other names
  • 1,4,5,8-Naphthalenetetracarboxylic dianhydride
  • Naphthalene-1,4,5,8-tetracarboxylic anhydride
Identifiers
CAS Number
  • 81-30-1 checkY
3D model (JSmol)
  • Interactive image
ChemSpider
  • 6426
ECHA InfoCard 100.001.221 Edit this at Wikidata
PubChem CID
  • 6678
UNII
  • L56XQD1V6Y checkY
CompTox Dashboard (EPA)
  • DTXSID4052554 Edit this at Wikidata
SMILES
  • C1=CC2=C3C(=CC=C4C3=C1C(=O)OC4=O)C(=O)OC2=O
Properties
Chemical formula
C14H4O6
Molar mass 268.180 g·mol−1
Appearance Beige powder
Melting point > 300 °C (572 °F; 573 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Naphthalenetetracarboxylic dianhydride (NTDA) is an organic compound related to naphthalene. The compound is a beige solid. NTDA is most commonly used as a precursor to naphthalenediimides (NDIs) (such as napthalenetetracarboxylic diimide), a family of compounds with many uses.[1]

  1. ^ Bhosale, Sheshanath V; Jani, Chintan H; Langford, Steven J (2008). "Chemistry of naphthalene diimides". Chem. Soc. Rev. 37 (2): 331. doi:10.1039/b615857a. PMID 18197349.

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Naphthalenetetracarboxylic dianhydride

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Naphthalenetetracarboxylic diimide

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from the parent naphthalene via an intermediate compound naphthalenetetracarboxylic dianhydride. NTCDI is redox-active, forming stable radical anions near...

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each of which are useful pigments. It is prepared from naphthalenetetracarboxylic dianhydride by condensation with o-phenylenediamine. The two Isomers...

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many applications. Naphthalenetetracarboxylic dianhydride, a building block for complex organic compounds, is an example of a dianhydride. Maleic anhydride...

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from condensation of the 1,2,4,5-tetraaminobenzene with naphthalenetetracarboxylic dianhydride. Some polysilicates are ladder polymers. One example is...

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