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Details

Stereochemistry ACHIRAL
Molecular Formula C12H8O4
Molecular Weight 216.1895
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2,6-NAPTHALENEDICARBOXYLIC ACID

SMILES

OC(=O)C1=CC2=CC=C(C=C2C=C1)C(O)=O

InChI

InChIKey=RXOHFPCZGPKIRD-UHFFFAOYSA-N
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)

HIDE SMILES / InChI
Molecular Formula C12H8O4
Molecular Weight 216.1895
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Unknown
149124
PubMed

PubMed

TitleDatePubMed
Naphthalene-2,6-dicarb-oxy-lic acid-1-methyl-pyrrolidin-2-one (1/2).
2010-12-24
Monitoring adsorption-induced switching by (129)Xe NMR spectroscopy in a new metal-organic framework Ni(2)(2,6-ndc)(2)(dabco).
2010-10-07
Influence of the photostabilizer in the photoprotective effects of a formulation containing UV-filters and vitamin A.
2010-10-01
A HPLC method to evaluate the influence of photostabilizers on cosmetic formulations containing UV-filters and vitamins A and E.
2010-09-15
Dissociation of dicarboxylate and disulfonate dianions.
2010-03-07
catena-Poly[bis[silver(I)-mu(2)-4,4'-bipyridine-kappa(2)N:N'] naphthalene-2,6-dicarboxylate tetrahydrate]: self-assembly of a supramolecular framework via coordination bonds and supramolecular interactions.
2009-11
Distinct differences in self-assembly of aromatic linear dicarboxylic acids.
2009-01-20
Framework reduction and alkali-metal doping of a triply catenating metal-organic framework enhances and then diminishes H2 uptake.
2009-01-06
Giant pores in a chromium 2,6-naphthalenedicarboxylate open-framework structure with MIL-101 topology.
2009
Multiple peak reference method for polarized Fourier transform infrared-attenuated total reflection spectroscopy to determine the three-dimensional orientation of a uniaxially drawn poly(trimethylene 2,6-naphthalate) film.
2008-12
Separation of CO2 from CH4 using mixed-ligand metal-organic frameworks.
2008-08-19
Selective three-phase liquid phase microextraction of acidic compounds from foodstuff simulants.
2008-07-11
Efficient hydrogen sorption in 8-connected MOFs based on trinuclear pinwheel motifs.
2008-06-16
A novel biotransformation of 2-formyl-6-naphthoic acid to 2,6-naphthalene dicarboxylic acid by Pseudomonas sp. for the purification of crude 2,6-naphthalene dicarboxylic acid.
2008-02
Poly[[μ(2)-aqua-tetraaquahexakis(μ(4)-naph-thalene-2,6-dicarboxylato)tetra-holmium(III)] 1.75-hydrate].
2008-01-11
Measurement of low-molecular-weight carboxylic acids in ambient air and vehicle emission by capillary electrophoresis.
2008
Poly[hexa-aqua-bis(μ(3)-naphthalene-2,6-dicarboxyl-ato)(μ(2)-naphthalene-2,6-dicarboxyl-ato)diholmium(III)].
2007-12-12
(Piperazin-1-ium-κN)tris-(thio-cyanato-κN)zinc(II).
2007-12-06
Selective gas sorption within a dynamic metal-organic framework.
2007-10-15
In-Silico docking of HIV-1 integrase inhibitors reveals a novel drug type acting on an enzyme/DNA reaction intermediate.
2007-03-20
Porous metal-organic framework with coordinatively unsaturated Mn(II) sites:sorption properties for various gases.
2006-10-16
Hydrogen adsorption in an interpenetrated dynamic metal-organic framework.
2006-07-24
Strong H(2) binding and selective gas adsorption within the microporous coordination solid Mg(3)(O(2)C-C(10)H(6)-CO(2))(3).
2005-07-06
Synthesis, X-ray crystal structures, and gas sorption properties of pillared square grid nets based on paddle-wheel motifs: implications for hydrogen storage in porous materials.
2005-06-06
Measurements of low-molecular-mass carboxylic acids in atmospheric aerosols by capillary electrophoresis.
2004-07
Hydrogen sorption in functionalized metal-organic frameworks.
2004-05-12
Surface-sensitive molecular information on polymers from UV-resonance Raman spectroscopy.
2003-05
Synthesis and characterization of gels from polyallylamine and carbon dioxide as gellant.
2003-04-30
Interactions of cyclodextrins with aromatic compounds studied by vibrational circular dichroism spectroscopy.
2002-11
Patents

Patents

JP1016823A
4
JP2000038532A
1
JP2000142659A
1
JP2000143788A
1
JP2000319364A
1
JP2000351861A
1
JP2000355625A
1
JP2001038866A
1
JP2002120345A
1
JP2002370276A
1
JP2002536519A
1
JP2003026629A
1
JP2003501532A
2
JP2006206663A
1
JP2010084065A
1
JP3395970B2
3
JP4190498B2
1
JP4520860B2
4
JPH00616835A
1
JPH01201324A
1
JPH01268661A
1
JPH01287055A
1
JPH0217131A
1
JPH02173058A
1
JPH02266939A
1
JPH02294329A
1
JPH02307788A
1
JPH0238422A
1
JPH03232837A
1
JPH03240751A
1
JPH04126220A
1
JPH04266851A
1
JPH04270240A
1
JPH05310922A
7
JPH05320325A
1
JPH06116487A
1
JPH06136228A
1
JPH06145319A
1
JPH06157403A
1
JPH06167776A
1
JPH06345859A
1
JPH06345863A
1
JPH0649190A
1
JPH07101906A
1
JPH07258406A
2
JPH08104743A
1
JPH08143653A
1
JPH08208955A
2
JPH083295A
1
JPH09151247A
1
JPH10110091A
1
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:22:19 GMT 2025
Edited
by admin
on Mon Mar 31 19:22:19 GMT 2025
Record UNII
K3C4DYZ29O
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2,6-NAPTHALENEDICARBOXYLIC ACID
Common Name English
NSC-96410
Preferred Name English
NAPHTHALENEDICARBOXYLIC ACID, 2,6-
Common Name English
2,6-NAPHTHALENE-DICARBOXYLIC ACID
Systematic Name English
2,6-NAPHTHALENEDICARBOXYLIC-ACID
Systematic Name English
2,6-NAPHTHALIC ACID
Common Name English
Classification Tree Code System Code
Food Contact Sustance Notif, (FCN No.) FCN NO. 135
Created by admin on Mon Mar 31 19:22:19 GMT 2025 , Edited by admin on Mon Mar 31 19:22:19 GMT 2025
Food Contact Sustance Notif, (FCN No.) FCN NO. 13
Created by admin on Mon Mar 31 19:22:19 GMT 2025 , Edited by admin on Mon Mar 31 19:22:19 GMT 2025
Food Contact Sustance Notif, (FCN No.) FCN. NO. 14
Created by admin on Mon Mar 31 19:22:19 GMT 2025 , Edited by admin on Mon Mar 31 19:22:19 GMT 2025
Code System Code Type Description
NSC
96410
Created by admin on Mon Mar 31 19:22:19 GMT 2025 , Edited by admin on Mon Mar 31 19:22:19 GMT 2025
PRIMARY
EPA CompTox
DTXSID5029211
Created by admin on Mon Mar 31 19:22:19 GMT 2025 , Edited by admin on Mon Mar 31 19:22:19 GMT 2025
PRIMARY
ECHA (EC/EINECS)
214-527-0
Created by admin on Mon Mar 31 19:22:19 GMT 2025 , Edited by admin on Mon Mar 31 19:22:19 GMT 2025
PRIMARY
CAS
1141-38-4
Created by admin on Mon Mar 31 19:22:19 GMT 2025 , Edited by admin on Mon Mar 31 19:22:19 GMT 2025
PRIMARY
FDA UNII
K3C4DYZ29O
Created by admin on Mon Mar 31 19:22:19 GMT 2025 , Edited by admin on Mon Mar 31 19:22:19 GMT 2025
PRIMARY
CHEBI
44460
Created by admin on Mon Mar 31 19:22:19 GMT 2025 , Edited by admin on Mon Mar 31 19:22:19 GMT 2025
PRIMARY
PUBCHEM
14357
Created by admin on Mon Mar 31 19:22:19 GMT 2025 , Edited by admin on Mon Mar 31 19:22:19 GMT 2025
PRIMARY
WIKIPEDIA
2,6-Naphthalenedicarboxylic acid
Created by admin on Mon Mar 31 19:22:19 GMT 2025 , Edited by admin on Mon Mar 31 19:22:19 GMT 2025
PRIMARY
NIH
NCATS
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