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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

2,7-Naphthalenedicarboxylic acid

OC(=O)c1ccc2c(c1)cc(cc2)C(=O)O Request for Quotation
Chemical Name: 2,7-Naphthalenedicarboxylic acid
CAS Number: 2089-89-6
Product Number: AG002JY6(AGN-PC-00G7YR)
Synonyms:
MDL No:
Molecular Formula: C12H8O4
Molecular Weight: 216.1895

Identification/Properties

Computed Properties
Molecular Weight:
216.192g/mol
XLogP3:
2.8
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
216.042g/mol
Monoisotopic Mass:
216.042g/mol
Topological Polar Surface Area:
74.6A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
271
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

PNMR/27-Naphtalendicarboxylic_acid-HNMR.pdf

Other Analytical Data

POTHER/27-Naphtalendicarboxylic_acid-HPLC.pdf

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Chemical Structure


Naphthalene-2,7-dicarboxylic acid, also known as NDA, functions as a versatile building block in chemical synthesis. Its unique structure and reactivity make it a valuable compound in the production of various chemicals and materials. NDA is commonly employed in the synthesis of pharmaceuticals, where it acts as a key intermediate in the creation of active pharmaceutical ingredients. Additionally, NDA is utilized in the development of specialty polymers and organic compounds, contributing to the advancement of materials science and industry applications. Its ability to undergo diverse chemical reactions enables the creation of novel molecules with tailored properties, further expanding its utility in synthetic chemistry.