1. Home
  2. Benzenesulfonamide, 4-methyl-N-8-quinolinyl-

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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)-

Benzenesulfonamide, 4-methyl-N-8-quinolinyl-

Cc1ccc(cc1)S(=O)(=O)Nc1cccc2c1nccc2 Request for Quotation
Chemical Name: Benzenesulfonamide, 4-methyl-N-8-quinolinyl-
CAS Number: 10304-39-9
Product Number: AG007Y6Q(AGN-PC-0JLTY3)
Synonyms:
MDL No:
Molecular Formula: C16H14N2O2S
Molecular Weight: 298.3596

Identification/Properties

Safety Information

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


4-Methyl-N-(quinolin-8-yl)benzenesulfonamide, also known as $name$, plays a crucial role in chemical synthesis as a versatile building block. This compound is commonly utilized as a key intermediate in the preparation of various pharmaceutical compounds and agrochemicals. Its unique chemical structure allows for strategic functionalization, making it valuable for the synthesis of complex molecules.In chemical synthesis, 4-Methyl-N-(quinolin-8-yl)benzenesulfonamide serves as a valuable starting material for the introduction of diverse functional groups through various synthetic transformations. It can undergo reactions such as halogenation, oxidation, reduction, and nucleophilic substitution to yield modified derivatives with tailored properties.The presence of the quinoline moiety in this compound offers opportunities for further diversification through heterocyclic chemistry. By exploiting the reactivity of quinoline, chemists can access a wide range of heterocyclic scaffolds, which are prevalent in pharmaceutical agents and bioactive molecules.Furthermore, the benzenesulfonamide group in 4-Methyl-N-(quinolin-8-yl)benzenesulfonamide provides an essential pharmacophore that is commonly found in drugs targeting various diseases. This motif contributes to the compound's biological activity and therapeutic potential, making it a valuable building block in drug discovery research.Overall, the application of 4-Methyl-N-(quinolin-8-yl)benzenesulfonamide in chemical synthesis lies in its versatility and reactivity, enabling the construction of structurally diverse compounds with potential pharmaceutical and agrochemical applications.