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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-bromophenyl)-

Brc1ccccc1NS(=O)(=O)C Request for Quotation
Chemical Name: Methanesulfonamide, N-(2-bromophenyl)-
CAS Number: 116547-91-2
Product Number: AG000CRM(AGN-PC-0KXN95)
Synonyms:
MDL No:
Molecular Formula: C7H8BrNO2S
Molecular Weight: 250.1129

Identification/Properties

Computed Properties
Molecular Weight:
250.11g/mol
XLogP3:
1.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
248.946g/mol
Monoisotopic Mass:
248.946g/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

NMR Spectrum

Other Analytical Data

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Chemical Structure


Methanesulfonamide, N-(2-bromophenyl)- is a versatile compound that finds wide applications in chemical synthesis. Primarily used as a powerful nucleophile, it is involved in various reactions to form new carbon-carbon or carbon-heteroatom bonds. This compound serves as an essential building block for the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. Additionally, its reactivity makes it a valuable reagent in the preparation of complex organic molecules through processes such as nucleophilic aromatic substitution and transition metal-catalyzed cross-coupling reactions. This compound's unique properties and versatility make it a valuable tool for chemists seeking to create novel compounds and advance the field of chemical synthesis.