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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, 4-acetyl-N-[(cyclohexylamino)carbonyl]-

O=C(NS(=O)(=O)c1ccc(cc1)C(=O)C)NC1CCCCC1 Request for Quotation
Chemical Name: Benzenesulfonamide, 4-acetyl-N-[(cyclohexylamino)carbonyl]-
CAS Number: 968-81-0
Product Number: AG005SIZ(AGN-PC-0JK633)
Synonyms:
MDL No:
Molecular Formula: C15H20N2O4S
Molecular Weight: 324.3953

Identification/Properties

Properties
MP:
>175°C (dec.)
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
324.395g/mol
XLogP3:
2.4
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
324.114g/mol
Monoisotopic Mass:
324.114g/mol
Topological Polar Surface Area:
101A^2
Heavy Atom Count:
22
Formal Charge:
0
Complexity:
498
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


4-Acetyl-N-[(cyclohexylamino)carbonyl]benzenesulfonamide is a valuable chemical compound widely employed in chemical synthesis processes. This versatile compound plays a crucial role in the development of pharmaceuticals, agrochemicals, and materials science. Its application in organic synthesis is particularly noteworthy, where it serves as a key intermediate in the production of various complex molecules.One of the primary uses of 4-Acetyl-N-[(cyclohexylamino)carbonyl]benzenesulfonamide is as a building block in the synthesis of sulfonamide derivatives. By reacting this compound with appropriate reagents, chemists can introduce specific functional groups or modify the structure to generate novel compounds with desired properties. The presence of both an acetyl group and a sulfonamide moiety in this molecule offers diverse opportunities for chemical transformations, making it a valuable tool in the creation of new substances.Furthermore, 4-Acetyl-N-[(cyclohexylamino)carbonyl]benzenesulfonamide is commonly utilized in medicinal chemistry for its ability to impart certain pharmacological activities to target compounds. Its presence in the synthesis of potential drug candidates allows researchers to explore structure-activity relationships and optimize the biological properties of the final molecules. This compound's structural characteristics make it an essential component in the design and development of therapeutic agents with improved efficacy and reduced side effects.In summary, the application of 4-Acetyl-N-[(cyclohexylamino)carbonyl]benzenesulfonamide in chemical synthesis is instrumental in advancing various fields of chemistry, enabling the creation of complex molecules, pharmaceuticals, and materials with enhanced properties and functionalities. Its versatility and reactivity make it a valuable asset for chemists seeking to explore new frontiers in organic synthesis and drug discovery.