665363

(S,R,R)-(+)-(3,5-Dioxa-4-phosphacyclohepta[2,1-a:3,4-a′]dinaphthalen-4-yl)bis(1-phenylethyl)amin

95% (HPLC)

• Synonym(e): (+)-N,N-Bis[(1R)-1-phenylethyl]-dinaphtho[2,1-d:1′,2′-f][1,3,2]dioxaphosphepin-4-amin, (11bS)
• Empirische Formel (Hill-System): C₃₆H₃₀NO₂P
• CAS-Nummer: 497883-22-4
• Molekulargewicht: 539.60
• MDL-Nummer: MFCD08561138
• UNSPSC-Code: 12352005
• PubChem Substanz-ID: 24884733
• NACRES: NA.22

Eigenschaften

• Qualitätsniveau: 100
• Assay: 95% (HPLC)
• mp (Schmelzpunkt): 102-103 °C
• Funktionelle Gruppe: amine; phenyl
• SMILES String: C[C@@H](N([C@H](C)c1ccccc1)P2Oc3ccc4ccccc4c3-c5c(O2)ccc6ccccc56)c7ccccc7
• InChI: 1S/C36H30NO2P/c1-25(27-13-5-3-6-14-27)37(26(2)28-15-7-4-8-16-28)40-38-33-23-21-29-17-9-11-19-31(29)35(33)36-32-20-12-10-18-30(32)22-24-34(36)39-40/h3-26H,1-2H3/t25-,26-/m1/s1
• InChIKey: LKZPDRCMCSBQFN-CLJLJLNGSA-N

Beschreibung

Anwendung

DSM MonoPhos Family of Highly Efficient Privileged Ligands

Chiral phosphoramidite ligand used in a highly enantioselective copper-catalyzed conjugate addition of diakylzincs to a variety of Michael acceptors. Also used in a palladium-catalyzed diethylzinc mediated umpolung allylation.

Leistungsmerkmale und Vorteile

Advantages of the MonoPhos^® ligands:

• Superior enantiocontrol in numerous transformations
• High activities at low catalyst loadings
• Hydrogenations under low-pressure conditions

Rechtliche Hinweise

Sold under license from DSM for research purposes only.

MonoPhos is a registered trademark of DSM IP Assets B.V.

Sicherheitshinweise

• Lagerklassenschlüssel: 11 - Combustible Solids
• WGK: WGK 3
• Flammpunkt (°F): Not applicable
• Flammpunkt (°C): Not applicable
• Persönliche Schutzausrüstung: Eyeshields, Gloves, type N95 (US)