1H-Imidazole, 2,4,5-tribromo-1-ethyl-


Chemical Name: 1H-Imidazole, 2,4,5-tribromo-1-ethyl-
CAS Number: 31250-75-6
Product Number: AG00BWWR(AGN-PC-0JNG8Q)
Synonyms:
MDL No:
Molecular Formula: C5H5Br3N2
Molecular Weight: 332.8186

Identification/Properties


Safety Information


GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum


Other Analytical Data


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Chemical Structure



The compound 2,4,5-Tribromo-1-ethyl-1H-imidazole plays a crucial role in chemical synthesis as a versatile building block. Its unique molecular structure, including the presence of three bromine atoms and an ethyl group attached to an imidazole ring, imparts specific reactivity and properties that are valuable in synthetic chemistry.In chemical synthesis, 2,4,5-Tribromo-1-ethyl-1H-imidazole is commonly used as a halogenated imidazole reagent for various transformations. Its bromine atoms can undergo substitution reactions with nucleophiles, facilitating the introduction of functional groups at specific positions in organic molecules. This reactivity makes it a valuable tool for synthesizing complex organic compounds with desired structural motifs.Furthermore, the ethyl group in 2,4,5-Tribromo-1-ethyl-1H-imidazole can serve as a versatile handle for further derivatization or coupling reactions. By selectively modifying the ethyl group, chemists can tailor the compound for specific applications or enhance its reactivity in various synthetic pathways.Overall, 2,4,5-Tribromo-1-ethyl-1H-imidazole's unique combination of bromine atoms and an ethyl group makes it a valuable building block in chemical synthesis, enabling the efficient construction of diverse organic molecules with tailored properties and functionalities.