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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)-

N-tert-butyl-3-(2-chloro-5-methylpyrimidin-4-ylamino)benzenesulfonamide

Clc1ncc(c(=Nc2cccc(c2)S(=O)(=O)NC(C)(C)C)[nH]1)C Request for Quotation
Chemical Name: N-tert-butyl-3-(2-chloro-5-methylpyrimidin-4-ylamino)benzenesulfonamide
CAS Number: 936092-53-4
Product Number: AG00H2YJ(AGN-PC-09RMO8)
Synonyms:
MDL No:
Molecular Formula: C15H19ClN4O2S
Molecular Weight: 354.8550

Identification/Properties

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound N-(tert-Butyl)-3-((2-chloro-5-methylpyrimidin-4-yl)amino)benzenesulfonamide is a versatile reagent used in chemical synthesis for its unique properties and functionalities. This compound is commonly employed as a building block in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. Its strategic placement of functional groups allows for efficient manipulation and modification in the synthesis of complex molecules. Specifically, the sulfonamide moiety can serve as a directing group in transition metal-catalyzed reactions, facilitating regioselective and stereoselective transformations. Additionally, the presence of the pyrimidine ring provides opportunities for further diversification through functional group interconversions. Overall, the application of N-(tert-Butyl)-3-((2-chloro-5-methylpyrimidin-4-yl)amino)benzenesulfonamide in chemical synthesis enables chemists to access new chemical entities with enhanced biological activities and properties.