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Structure of 1088-00-2
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5-Phenyl-5H-benzo[b]phosphindole features a rigid, electron-rich heterocyclic core with a phosphorus atom at the bridgehead position, enabling stable coordination in transition metal catalysis. The phenyl substituent enhances π-conjugation and solubility, while the scaffold's steric profile supports selective ligand design for palladium and nickel systems. This compound integrates readily into catalytic cycles requiring robust, bulky phosphine-like functionality.
5-Phenyl-5H-benzo[b]phosphindole serves as a versatile heterocyclic scaffold in medicinal chemistry, featuring a phosphorus-containing core with inherent stability and favorable electronic properties. It functions as a key building block for transition-metal-catalyzed coupling reactions, enabling efficient construction of complex molecular architectures. The phenyl substitution enhances π-conjugation and provides orthogonal functionalization potential, supporting downstream derivatization in drug discovery workflows. Its bench-stable nature and compatibility with standard synthetic protocols make it well-suited for high-throughput applications.
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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 : H315-H319
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Precautionary Statements : P264-P280-P302+P352-P362+P364
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Lot numbers can be found on the outside label of a product: