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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)-

Methanesulfonamide, N-(2-fluorophenyl)-

Fc1ccccc1NS(=O)(=O)C Request for Quotation
Chemical Name: Methanesulfonamide, N-(2-fluorophenyl)-
CAS Number: 98611-90-6
Product Number: AG003S9G(AGN-PC-0JUOMW)
Synonyms:
MDL No:
Molecular Formula: C7H8FNO2S
Molecular Weight: 189.2073232

Identification/Properties

Computed Properties
Molecular Weight:
189.204g/mol
XLogP3:
1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
189.026g/mol
Monoisotopic Mass:
189.026g/mol
Topological Polar Surface Area:
54.6A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
234
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


N-(2-Fluorophenyl)methanesulfonamide is a versatile compound widely utilized in chemical synthesis as a key building block for the development of various pharmaceuticals, agrochemicals, and materials. This compound serves as a crucial intermediate in the production of organic compounds due to its unique structure and reactivity. In chemical synthesis, N-(2-Fluorophenyl)methanesulfonamide is commonly employed as a nucleophile or as a source of the sulfonamide functional group, allowing for the introduction of the fluorophenyl and sulfonamide motifs into target molecules. Its ability to participate in a variety of synthetic transformations makes it an indispensable tool for the creation of complex organic molecules with diverse applications. Furthermore, the presence of the fluorine atom in this compound enhances its utility in medicinal chemistry by providing the potential for controlling biological activities and improving pharmacokinetic properties of the final products.