5-Bromo-4-chloro-2-fluoro-benzenesulfonyl chloride


Chemical Name: 5-Bromo-4-chloro-2-fluoro-benzenesulfonyl chloride
CAS Number: 1070972-67-6
Product Number: AG0091SQ(AGN-PC-0WP1P3)
Synonyms:
MDL No:
Molecular Formula: C6H2BrCl2FO2S
Molecular Weight: 307.9523

Identification/Properties


Safety Information


GHS Pictogram:
Signal Word:
Danger
UN#:
3261
Hazard Statements:
H302-H314
Precautionary Statements:
P261-P280-P305+P351+P338-P310
Class:
8
Packing Group:

NMR Spectrum


Other Analytical Data


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Chemical Structure



5-Bromo-4-Chloro-2-fluorobenzene-1-sulfonyl chloride, also known as $name$, is a versatile chemical compound widely utilized in chemical synthesis processes. This sulfonyl chloride derivative is valued for its ability to function as a reactive intermediate in various reactions, making it a crucial component in the production of pharmaceuticals, agrochemicals, and advanced materials.In chemical synthesis, $name$ is commonly employed as a sulfonating agent due to its high reactivity towards nucleophiles. This reactivity allows for the introduction of the sulfonyl group into organic molecules, enabling the modification of their physicochemical properties. Additionally, $name$ serves as a key building block in the synthesis of complex organic compounds by participating in cross-coupling reactions, nucleophilic substitutions, and other transformations.Furthermore, the unique combination of bromine, chlorine, and fluorine atoms in the molecular structure of $name$ confers specific reactivity and selectivity in various synthetic pathways. This enables chemists to tailor the properties of the target molecules, leading to the development of novel compounds with enhanced functionalities.Overall, the application of 5-Bromo-4-Chloro-2-fluorobenzene-1-sulfonyl chloride in chemical synthesis underscores its significance in creating diverse molecular architectures and facilitating the discovery of new materials with potential industrial applications.