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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)-

Benzenesulfonyl chloride, formyl-

O=Cc1ccccc1S(=O)(=O)Cl Request for Quotation
Chemical Name: Benzenesulfonyl chloride, formyl-
CAS Number: 21639-41-8
Product Number: AG00BSBM(AGN-PC-0JKLIZ)
Synonyms:
MDL No:
Molecular Formula: C7H5ClO3S
Molecular Weight: 204.6308

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NMR Spectrum

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Chemical Structure


2-Formylbenzene-1-sulfonyl chloride, also known as Benzenesulfonyl chloride, is a versatile compound widely used in chemical synthesis as a key building block in the preparation of various pharmaceuticals, agrochemicals, and specialty chemicals. This compound is particularly valuable in organic synthesis due to its unique reactivity and ability to introduce the sulfonyl functional group into target molecules. It can be utilized as a sulfonylating agent in the production of sulfonamides, sulfonates, and sulfonylureas, which are important classes of compounds with diverse applications in medicinal chemistry and materials science. Furthermore, 2-Formylbenzene-1-sulfonyl chloride can serve as a powerful acylating agent in synthetic pathways, facilitating the introduction of the formyl group into organic molecules to create aldehydes, ketones, and carboxylic acids. Its selective reactivity and compatibility with a wide range of functional groups make it a valuable tool for chemists seeking to build complex molecular architectures efficiently and selectively.