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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)-

Benzenesulfonic acid, 2-chloro-5-nitro-, sodium salt

[O-][N+](=O)c1ccc(c(c1)S(=O)(=O)[O-])Cl.[Na+] Request for Quotation
Chemical Name: Benzenesulfonic acid, 2-chloro-5-nitro-, sodium salt
CAS Number: 946-30-5
Product Number: AG00H5QG(AGN-PC-0W48KB)
Synonyms:
MDL No:
Molecular Formula: C6H3ClNNaO5S
Molecular Weight: 259.5995

Identification/Properties

Properties
MP:
>300°C
Storage:
Keep in dry area;-10 ℃;Inert atmosphere;
Computed Properties
Molecular Weight:
259.592g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
0
Exact Mass:
258.932g/mol
Monoisotopic Mass:
258.932g/mol
Topological Polar Surface Area:
111A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
305
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 2-chloro-5-nitrobenzenesulfonate is a versatile chemical compound widely used in chemical synthesis. This compound serves as an important reagent in organic chemistry, particularly in the field of sulfonation reactions. Its application in chemical synthesis involves the introduction of sulfonyl groups into various organic molecules, which can lead to the creation of new functionalized compounds with valuable properties.In organic synthesis, sodium 2-chloro-5-nitrobenzenesulfonate is commonly employed for sulfonylation reactions, where the sulfonate group is added to a target molecule. This process can be utilized to modify the properties of organic molecules, such as altering their solubility, stability, or reactivity. Additionally, the presence of the nitro group in the compound can further enhance the reactivity and selectivity of the sulfonation reaction.Furthermore, the use of sodium 2-chloro-5-nitrobenzenesulfonate in chemical synthesis enables the efficient functionalization of aromatic compounds, leading to the synthesis of various intermediates and final products with tailored properties. This compound plays a crucial role in the preparation of pharmaceuticals, agrochemicals, dyes, and other fine chemicals by enabling the introduction of specific functional groups in a controlled manner.Overall, the application of sodium 2-chloro-5-nitrobenzenesulfonate in chemical synthesis offers chemists a powerful tool for the strategic modification of organic molecules, facilitating the synthesis of diverse compounds with desired properties for various industrial and research applications.