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Structure of 1373432-13-3
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(2S,3S)-2-Benzyl-3-(tert-butyl)-4-(2,6-dimethoxyphenyl)phosphole features a chiral phosphole core with orthogonal functionalization: a benzyl group at C2, a tert-butyl moiety at C3, and a 2,6-dimethoxyphenyl substituent at C4. This configuration imparts enhanced stability and stereochemical integrity, enabling its use in asymmetric synthesis and catalytic applications where controlled steric and electronic environments are critical.
(2S,3S)-2-Benzyl-3-(tert-butyl)-4-(2,6-dimethoxyphenyl)phosphole serves as a stable, bench-ready chiral phosphole scaffold enabling stereoselective cross-coupling reactions. Its functional group tolerance and robustness under standard transition-metal catalysis facilitate efficient access to complex phosphorus-containing architectures. The tert-butyl and benzyl substituents enhance solubility and stability, while the 2,6-dimethoxyphenyl group provides electronic modulation and compatibility with Pd-catalyzed transformations. This compound functions as a versatile building block in the synthesis of bioactive heterocycles and ligands for asymmetric catalysis.
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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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: