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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)-

3-Pyridinesulfonic acid, sodium salt

[O-]S(=O)(=O)c1cccnc1.[Na+] Request for Quotation
Chemical Name: 3-Pyridinesulfonic acid, sodium salt
CAS Number: 15521-77-4
Product Number: AG001NQK(AGN-PC-0WALVV)
Synonyms:
MDL No:
Molecular Formula: C5H4NNaO3S
Molecular Weight: 181.1449

Identification/Properties

Properties
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
181.141g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
180.981g/mol
Monoisotopic Mass:
180.981g/mol
Topological Polar Surface Area:
78.5A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
198
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


Sodium pyridine-3-sulfonate plays a crucial role in chemical synthesis as a versatile reagent with a wide range of applications. This compound is commonly used as a key building block in organic synthesis, particularly in the preparation of various pharmaceuticals, agrochemicals, and fine chemicals. Its unique structure and reactivity make it a valuable intermediate for the synthesis of heterocyclic compounds and functionalized organic molecules. Sodium pyridine-3-sulfonate serves as a valuable tool in the development of new chemical processes, offering chemists the ability to introduce pyridine and sulfonate functionalities into diverse molecular frameworks. Its ability to participate in a variety of chemical transformations, including nucleophilic substitution and metal-catalyzed reactions, makes it a highly sought-after reagent for synthetic chemists aiming to access novel compounds with tailored properties.