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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)-

Benzenesulfonamide, N-(3-bromophenyl)-

Brc1cccc(c1)NS(=O)(=O)c1ccccc1 Request for Quotation
Chemical Name: Benzenesulfonamide, N-(3-bromophenyl)-
CAS Number: 91394-73-9
Product Number: AG00IGMZ(AGN-PC-0JNX66)
Synonyms:
MDL No:
Molecular Formula: C12H10BrNO2S
Molecular Weight: 312.1823

Identification/Properties

Computed Properties
Molecular Weight:
312.181g/mol
XLogP3:
3.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
310.962g/mol
Monoisotopic Mass:
310.962g/mol
Topological Polar Surface Area:
54.6A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
333
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

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

NMR Spectrum

Other Analytical Data

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Chemical Structure


N-(3-Bromophenyl)benzenesulfonamide, also known as $name$, is a valuable compound widely used in chemical synthesis. Its unique structure and reactivity make it a versatile building block for the preparation of various organic compounds. In chemical synthesis, $name$ is commonly employed as a key intermediate in the production of pharmaceuticals, agrochemicals, and other specialty chemicals.One of the primary applications of N-(3-Bromophenyl)benzenesulfonamide is in the formation of C-N bonds through amidation reactions. By reacting with a wide range of amines, this compound serves as an efficient coupling reagent to introduce the sulfonamide moiety into the target molecules. This strategy allows for the functionalization of organic molecules with enhanced biological activities or specific chemical properties.Moreover, $name$ can participate in transition metal-catalyzed cross-coupling reactions, such as the Suzuki-Miyaura, Heck, or Buchwald-Hartwig reactions. These transformations enable the rapid and selective formation of biaryl and aryl-aryl linkages, leading to the construction of complex molecular architectures. The presence of the bromophenyl group in the structure of N-(3-Bromophenyl)benzenesulfonamide further facilitates ortho-metalation reactions, enhancing its versatility in synthetic methodologies.Additionally, the sulfonamide functionality in N-(3-Bromophenyl)benzenesulfonamide can serve as a directing group in various C-H activation processes. This feature allows for the selective functionalization of specific C-H bonds in aromatic and heteroaromatic compounds, enabling the rapid diversification of chemical structures with high regioselectivity.Overall, the application of N-(3-Bromophenyl)benzenesulfonamide in chemical synthesis demonstrates its significance as a valuable building block for the construction of diverse organic molecules with medicinal, agricultural, and material science applications.