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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, 2-bromo-

Brc1ccccc1S(=O)(=O)N Request for Quotation
Chemical Name: Benzenesulfonamide, 2-bromo-
CAS Number: 92748-09-9
Product Number: AG006158(AGN-PC-0KLBO0)
Synonyms:
MDL No:
Molecular Formula: C6H6BrNO2S
Molecular Weight: 236.0863

Identification/Properties

Properties
MP:
192-193 °C
BP:
374.5°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
236.083g/mol
XLogP3:
0.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
234.93g/mol
Monoisotopic Mass:
234.93g/mol
Topological Polar Surface Area:
68.5A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
221
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-P280-P301+P312-P302+P352-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Bromobenzenesulfonamide is a versatile chemical reagent frequently utilized in chemical synthesis for its unique properties and reactions. In particular, this compound is commonly employed as a potent electrophilic halogenating agent in various organic transformations. Due to its high reactivity, 2-bromobenzenesulfonamide enables efficient introduction of the bromine atom into organic molecules, facilitating the synthesis of diverse brominated compounds with precision and control. This reagent's ability to undergo selective and high-yielding reactions makes it a valuable tool for medicinal chemistry, material science, and the preparation of complex organic molecules. Its application in the synthesis of pharmaceuticals, agrochemicals, and advanced materials underscores its significance in modern chemical research and development.