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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)-

6-Quinolinesulfonyl chloride, 1,2-dihydro-2-oxo-

O=c1ccc2c([nH]1)ccc(c2)S(=O)(=O)Cl Request for Quotation
Chemical Name: 6-Quinolinesulfonyl chloride, 1,2-dihydro-2-oxo-
CAS Number: 569340-07-4
Product Number: AG00IA5P(AGN-PC-09RW3S)
Synonyms:
MDL No:
Molecular Formula: C9H6ClNO3S
Molecular Weight: 243.6668

Identification/Properties

Safety Information

GHS Pictogram:
Signal Word:
Danger
UN#:
1759
Hazard Statements:
H302-H314
Precautionary Statements:
P261-P280-P305+P351+P338-P310
Class:
8
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Hydroxyquinoline-6-sulfonyl chloride, also known as $name$, is a versatile reagent widely used in chemical synthesis for its unique properties and broad range of applications. As a sulfonyl chloride derivative of 2-hydroxyquinoline, this compound serves as a valuable building block in the synthesis of diverse organic molecules.One of the key applications of $name$ is in the synthesis of various heterocyclic compounds. By acting as a sulfonylating agent, it can introduce the sulfonyl group onto aromatic rings, enabling the formation of complex ring structures with enhanced reactivity and functionality. This makes $name$ particularly useful in the preparation of pharmaceuticals, agrochemicals, and materials with tailored properties.Moreover, 2-Hydroxyquinoline-6-sulfonyl chloride exhibits high reactivity towards nucleophiles, allowing for selective derivatization of hydroxyquinoline moieties. This reactivity opens up possibilities for the creation of new molecular entities with specific biological activities or functional properties.In addition to its role in heterocyclic chemistry, $name$ is also employed as a key intermediate in the synthesis of fluorescent probes, coordination complexes, and ligands for transition metal catalysis. Its ability to participate in diverse chemical transformations makes it a valuable tool for organic chemists seeking to design and construct novel molecules for various applications.Overall, the versatility and reactivity of 2-Hydroxyquinoline-6-sulfonyl chloride make it a valuable reagent in chemical synthesis, offering opportunities for the development of innovative compounds with tailored properties and functions.