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Structure of 221636-18-6
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5-Bromo-1-phenyl-1H-benzo[d]imidazole features a brominated benzimidazole core paired with a phenyl substituent, delivering enhanced electronic and steric profile for use in cross-coupling reactions. The electron-deficient imidazole ring facilitates palladium-catalyzed transformations, while the bromine handle enables efficient functionalization. This bench-stable compound serves as a key building block in synthetic organic chemistry and materials science applications.
5-Bromo-1-phenyl-1H-benzo[d]imidazole serves as a versatile building block in heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions due to its well-defined bromine handle. The molecule exhibits excellent bench stability and compatibility with standard reaction conditions, facilitating efficient functionalization at the 5-position. Its rigid aromatic core and defined substitution pattern support predictable reactivity in the construction of complex scaffolds relevant to medicinal chemistry and materials science.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: