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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-Naphthalenesulfonylchloride, 7-chloro-

Clc1ccc2c(c1)cc(cc2)S(=O)(=O)Cl Request for Quotation
Chemical Name: 2-Naphthalenesulfonylchloride, 7-chloro-
CAS Number: 102153-64-0
Product Number: AG0006QW(AGN-PC-0N6NA7)
Synonyms:
MDL No:
Molecular Formula: C10H6Cl2O2S
Molecular Weight: 261.1244

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Chemical Structure


7-Chloro-2-naphthalenesulfonyl chloride is a versatile chemical reagent commonly used in organic synthesis as a sulfonylating agent. Its ability to introduce a sulfonyl group onto various nucleophiles makes it a valuable tool in the preparation of sulfonamides, sulfones, and sulfonates. This reagent is particularly useful in the synthesis of pharmaceuticals, agrochemicals, and advanced materials due to the wide range of reactions it can participate in. In addition, 7-Chloro-2-naphthalenesulfonyl chloride is known for its high reactivity and selectivity, making it a preferred choice for chemists working on complex synthetic transformations. Its straightforward handling and compatibility with a variety of reaction conditions further enhance its utility in chemical synthesis.