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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)-

2,6-Naphthalenedisulfonic acid, disodium salt

[O-]S(=O)(=O)c1ccc2c(c1)ccc(c2)S(=O)(=O)[O-].[Na+].[Na+] Request for Quotation
Chemical Name: 2,6-Naphthalenedisulfonic acid, disodium salt
CAS Number: 1655-45-4
Product Number: AG001W6J(AGN-PC-0Q8R69)
Synonyms:
MDL No:
Molecular Formula: C10H6Na2O6S2
Molecular Weight: 332.2606

Identification/Properties

Properties
MP:
>300 °C(lit.)
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
332.252g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
0
Exact Mass:
331.94g/mol
Monoisotopic Mass:
331.94g/mol
Topological Polar Surface Area:
131A^2
Heavy Atom Count:
20
Formal Charge:
0
Complexity:
423
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:
3
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2,6-Naphthalenedisulfonic acid disodium salt, also known as $name$, is a versatile compound widely used in chemical synthesis. This compound plays a crucial role in the preparation of various dyes and pigments due to its strong acidic nature and sulfonic acid groups. One of the primary applications of $name$ in chemical synthesis is its use as a key intermediate in the production of azo dyes. By reacting $name$ with aromatic amines, diazonium salts can be formed, which then undergo azo coupling reactions to yield vibrant and stable azo dyes. Additionally, $name$ can also be employed in the synthesis of pharmaceuticals and fluorescent compounds. Its sulfonic acid groups allow for easy water solubility, making it a valuable reagent in solution-phase chemistry. Furthermore, the presence of multiple sulfonic acid groups enhances the compound's chelating capabilities, leading to its use in metal complexation reactions and as a catalyst in organic transformations.