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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)-

Aziridine, 1-[(4-methylphenyl)sulfonyl]-2-phenyl-

Cc1ccc(cc1)S(=O)(=O)N1CC1c1ccccc1 Request for Quotation
Chemical Name: Aziridine, 1-[(4-methylphenyl)sulfonyl]-2-phenyl-
CAS Number: 24395-14-0
Product Number: AG019O0F(AGN-PC-0JT5ZR)
Synonyms:
MDL No:
Molecular Formula: C15H15NO2S
Molecular Weight: 273.3501

Identification/Properties

Computed Properties
Molecular Weight:
273.35g/mol
XLogP3:
2.7
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
273.082g/mol
Monoisotopic Mass:
273.082g/mol
Topological Polar Surface Area:
45.5A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
400
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-(4-Methylbenzenesulfonyl)-2-phenylaziridine is a versatile compound that finds widespread application in chemical synthesis. This particular aziridine derivative serves as a valuable building block in the creation of various chemical compounds due to its unique structural properties. Its sulfonamide and aryl groups play crucial roles in enabling diverse reactions and allowing for the formation of complex molecular structures.In chemical synthesis, 1-(4-Methylbenzenesulfonyl)-2-phenylaziridine is particularly prized for its ability to undergo ring-opening reactions, nucleophilic substitutions, and cyclization processes. These reactions enable the introduction of functional groups or the modification of existing substituents, providing chemists with a range of possibilities for designing molecules with specific properties.Furthermore, its aziridine ring contains a strained three-membered structure that allows for transformations leading to the formation of heterocyclic compounds. This feature makes 1-(4-Methylbenzenesulfonyl)-2-phenylaziridine an essential component in the synthesis of pharmaceuticals, agrochemicals, and advanced materials where the presence of aziridine motifs is crucial for biological activity or material properties.Overall, the versatile nature of 1-(4-Methylbenzenesulfonyl)-2-phenylaziridine makes it a valuable tool for chemists engaged in the synthesis of complex molecules, providing a platform for creativity and innovation in the field of chemical science.