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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)-

1-Naphthalenesulfonic acid, sodium salt

[O-]S(=O)(=O)c1cccc2c1cccc2.[Na+] Request for Quotation
Chemical Name: 1-Naphthalenesulfonic acid, sodium salt
CAS Number: 130-14-3
Product Number: AG000TUT(AGN-PC-0PJ521)
Synonyms:
MDL No:
Molecular Formula: C10H7NaO3S
Molecular Weight: 230.2155

Identification/Properties

Properties
MP:
299-301 °C
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Stability:
Hygroscopic
Computed Properties
Molecular Weight:
230.213g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
230.001g/mol
Monoisotopic Mass:
230.001g/mol
Topological Polar Surface Area:
65.6A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
296
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:
2
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


The application of Sodium 1-naphthalenesulfonate in chemical synthesis is significant due to its versatile properties. This compound serves as a highly valuable reagent in various organic reactions, particularly in the field of organic chemistry. Sodium 1-naphthalenesulfonate acts as a nucleophile in substitution reactions, where it can displace other functional groups or elements in a molecule. Additionally, it can be utilized as a catalyst in certain transformations, enabling the facilitation of specific chemical processes.In addition to its role as a reagent and catalyst, Sodium 1-naphthalenesulfonate also exhibits surfactant properties, making it useful in emulsion polymerization reactions. Its ability to lower the surface tension between different phases allows for more efficient mixing and reaction between reactants. This aspect is particularly advantageous in the synthesis of polymers and other complex organic compounds.Moreover, Sodium 1-naphthalenesulfonate can serve as a stabilizer in various chemical reactions, helping to control the rate of reaction or prevent undesired side reactions. Its presence can influence the overall yield and selectivity of the desired product in a synthesis process. Overall, Sodium 1-naphthalenesulfonate plays a crucial role in facilitating diverse chemical transformations and is a valuable tool in the realm of chemical synthesis.