2,6-Naphthalenedicarboxylic acid

2,6-Naphthalenedicarboxylic acid
Names
	Preferred IUPAC name Naphthalene-2,6-dicarboxylic acid
	Other names 2,6-Naphthalenedicarboxylic acid
Identifiers
CAS Number	1141-38-4;
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:44460;
ChemSpider	13718;
ECHA InfoCard	100.013.206
EC Number	214-527-0;
PubChem CID	14357;
CompTox Dashboard (EPA)	DTXSID5029211 ;
	InChI InChI=1S/C12H8O4/c13-11(14)9-3-1-7-5-10(12(15)16)4-2-8(7)6-9/h1-6H,(H,13,14)(H,15,16) Key: RXOHFPCZGPKIRD-UHFFFAOYSA-N;
	SMILES C1=CC2=C(C=CC(=C2)C(=O)O)C=C1C(=O)O;
Properties
Chemical formula	C12H8O4
Molar mass	216.192 g·mol−1
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

2,6-Naphthalenedicarboxylic acid is an organic compound with the formula C₁₀H₆(CO₂H)₂. This colorless solid is one of several isomers of naphthalenedicarboxylic acid. It is a precursor to the high performance polyester polyethylene naphthalate (PEN, poly(ethylene-2,6-naphthalene dicarboxylate)).^[1] It is also used in the synthesis of metal-organic frameworks.

References

^ Lillwitz, L. D. (2001). "Production of Dimethyl-2,6-Naphthalenedicarboxylate: Precursor to Polyethylene Naphthalate". Applied Catalysis, A: General. 221: =337–358. doi:10.1016/S0926-860X(01)00809-2.{{cite journal}}: CS1 maint: extra punctuation (link)

This article about an aromatic compound is a stub. You can help Wikipedia by expanding it.

[1] Lillwitz, L. D. (2001). "Production of Dimethyl-2,6-Naphthalenedicarboxylate: Precursor to Polyethylene Naphthalate". Applied Catalysis, A: General. 221: =337–358. doi:10.1016/S0926-860X(01)00809-2.{{cite journal}}: CS1 maint: extra punctuation (link)

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