Benzenesulfonamide, 4-(bromoacetyl)-N,N-dimethyl-


Chemical Name: Benzenesulfonamide, 4-(bromoacetyl)-N,N-dimethyl-
CAS Number: 89102-54-5
Product Number: AG003ZM3(AGN-PC-0LK8WG)
Synonyms:
MDL No:
Molecular Formula: C10H12BrNO3S
Molecular Weight: 306.1762

Identification/Properties


Computed Properties
Molecular Weight:
306.174g/mol
XLogP3:
1.5
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
304.972g/mol
Monoisotopic Mass:
304.972g/mol
Topological Polar Surface Area:
62.8A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
340
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



Benzenesulfonamide, 4-(2-bromoacetyl)-N,N-dimethyl- is a versatile compound commonly used in chemical synthesis for a wide range of applications. This compound serves as a valuable building block in organic chemistry reactions due to its unique structural properties. Its bromoacetyl functional group allows for selective derivatization and modification, making it a key intermediate in the synthesis of various pharmaceuticals, agrochemicals, and materials.In organic synthesis, Benzenesulfonamide, 4-(2-bromoacetyl)-N,N-dimethyl- is often employed as a versatile reagent for introducing the bromoacetyl group into complex molecules. The presence of the bromoacetyl moiety enables further functionalization through nucleophilic substitution, acylation, and condensation reactions, thereby facilitating the construction of diverse molecular architectures. This compound's dimethyl sulfonamide backbone also provides additional stability and compatibility with a wide range of reaction conditions, enhancing its utility in synthetic methodologies.By incorporating Benzenesulfonamide, 4-(2-bromoacetyl)-N,N-dimethyl- into chemical reactions, researchers and chemists can efficiently access structurally complex and biologically active compounds. Its strategic placement within a molecular framework enables precise control over the introduction of functional groups, enabling the synthesis of target molecules with high selectivity and efficiency. Whether used in drug discovery, materials science, or agrochemical development, this compound offers synthetic chemists a versatile tool for molecular design and manipulation.