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Structure of 16096-33-6
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1-Phenyl-1H-indole features a fused bicyclic core with an appended phenyl group, enhancing π-conjugation and enabling applications in organic synthesis and materials science. This bench-stable heterocycle integrates readily into complex scaffolds, offering predictable reactivity in electrophilic substitution and transition-metal-catalyzed coupling processes.
1-Phenyl-1H-indole serves as a versatile scaffold in medicinal chemistry and materials science, enabling efficient construction of biologically active heterocycles. Its robust indole core exhibits favorable bench stability and compatibility with standard functionalization protocols, including electrophilic substitution and transition-metal-catalyzed coupling reactions. The molecule functions effectively as a building block for pharmaceutical intermediates and fluorescent probes due to its extended π-conjugation and predictable reactivity profile.
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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: