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Structure of 134532-03-9
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2'-Amino[1,1'-binaphthalen]-2-ol features a rigid binaphthyl scaffold with strategically positioned amino and phenolic hydroxyl groups. This arrangement enables strong chelation in asymmetric catalysis and facilitates directional π-stacking interactions. The compound exhibits enhanced solubility in polar solvents and stability under standard bench conditions, making it well-suited for ligand design in transition metal complexes.
2'-Amino[1,1'-binaphthalen]-2-ol serves as a versatile chiral scaffold for asymmetric synthesis, featuring a rigid binaphthyl backbone with ortho-hydroxyl and amino functionalities. The phenolic OH enables metal coordination and hydrogen bonding, while the amino group facilitates derivatization and acts as a directing group in transition-metal-catalyzed reactions. Its bench-stable nature and compatibility with standard coupling protocols make it a practical building block for ligands, catalysts, and functionalized heterocycles in medicinal chemistry and catalysis.
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GHS Pictogram :
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GHS No : GHS05
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Signal Word : Danger
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UN#: 3077
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Class : 9
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Packing Group : Ⅲ
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Hazard Statements : H303-H318-H410
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Precautionary Statements : P280-P391-P501
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Lot numbers can be found on the outside label of a product: