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Names | |
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Preferred IUPAC name
Naphthalene-2,6-dicarboxylic acid | |
Other names
2,6-Naphthalenedicarboxylic acid
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Identifiers | |
3D model (
JSmol)
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ChEBI | |
ChemSpider | |
ECHA InfoCard | 100.013.206 |
EC Number |
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PubChem
CID
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UNII | |
CompTox Dashboard (
EPA)
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Properties | |
C12H8O4 | |
Molar mass | 216.192 g·mol−1 |
Appearance | colorless solid |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
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 some metal-organic frameworks.
The conjugate base of 2,6-naphthalenedicarboxylic acid, when heated, isomerizes to the 1,6-isomer, which is readily converted to 1,6-naphthalenedicarboxylic acid. [2] It is also produced by oxidation of 2,6-diisopropylnaphthalene. [3]
![]() | |
Names | |
---|---|
Preferred IUPAC name
Naphthalene-2,6-dicarboxylic acid | |
Other names
2,6-Naphthalenedicarboxylic acid
| |
Identifiers | |
3D model (
JSmol)
|
|
ChEBI | |
ChemSpider | |
ECHA InfoCard | 100.013.206 |
EC Number |
|
PubChem
CID
|
|
UNII | |
CompTox Dashboard (
EPA)
|
|
| |
| |
Properties | |
C12H8O4 | |
Molar mass | 216.192 g·mol−1 |
Appearance | colorless solid |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
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 some metal-organic frameworks.
The conjugate base of 2,6-naphthalenedicarboxylic acid, when heated, isomerizes to the 1,6-isomer, which is readily converted to 1,6-naphthalenedicarboxylic acid. [2] It is also produced by oxidation of 2,6-diisopropylnaphthalene. [3]