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500997-70-6

Diindeno[7,1-de:1',7'-fg][1,3,2]dioxaphosphocin-5-amine,10,11,12,13-tetrahydro-N,N-bis[(1R)-1-phenylethyl]-, (11aS)-

Catalog#: AR00DDOR  |   CAS#: 500997-70-6  |   MDL#: MFCD08459342  |   MF: C66H64N2O4P2  |   MW: 1011.1729

Packsize Purity Price Availability Quantity
25mg 98% $19.00 Global Stock Buy Now Add To Cart
50mg 98% $33.00 Global Stock Buy Now Add To Cart
100mg 98% $43.00 Global Stock Buy Now Add To Cart
250mg 98% $108.00 Global Stock Buy Now Add To Cart
1g 98% $347.00 Global Stock Buy Now Add To Cart
5g 98% $1,276.00 Global Stock Buy Now Add To Cart
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Catalog Number AR00DDOR
Chemical Name Diindeno[7,1-de:1',7'-fg][1,3,2]dioxaphosphocin-5-amine,10,11,12,13-tetrahydro-N,N-bis[(1R)-1-phenylethyl]-, (11aS)-
CAS Number 500997-70-6
Molecular Formula C66H64N2O4P2
Molecular Weight 1011.1729
MDL Number MFCD08459342
SMILES C[C@@H](N([C@@H](c1ccccc1)C)P1Oc2cccc3c2C2(c4c(O1)cccc4CC2)CC3)c1ccccc1.C[C@@H](N([C@@H](c1ccccc1)C)P1Oc2cccc3c2C2(c4c(O1)cccc4CC2)CC3)c1ccccc1

The compound (11aS)-(-)-10,11,12,13-Tetrahydrodiindeno[7,1-de:1',7'-fg][1,3,2]dioxaphosphocin-5-bis[(R)-1-phenylethyl]amine is widely used in chemical synthesis as a chiral ligand for catalytic reactions. Its unique structure provides a highly selective environment for various asymmetric transformations, making it particularly valuable in organic synthesis. This compound is commonly employed in transition metal-catalyzed reactions to facilitate the formation of key chiral intermediates with high enantioselectivity. Its ability to control the stereochemistry of reactions makes it a powerful tool in the preparation of complex molecules with specific three-dimensional arrangements. Furthermore, the compound's versatile nature allows for its application in a variety of synthetic methodologies, contributing to the advancement of diverse chemical processes.
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