693022

S-DM-BINAP

• Sinonimo/i: S-(−)-2,2′-Bis[di(3,5-xylyl)phoshino]-1,1′-binaphthyl
• Formula empirica (notazione di Hill): C₅₂H₄₈P₂
• Numero CAS: 135139-00-3
• Peso molecolare: 734.89
• Numero MDL: MFCD01630821
• Codice UNSPSC: 12352005
• ID PubChem: 329761554

Proprietà

• Stato: solid
• Attività ottica: [α]/D -172°, 20, c = 1 in chloroform
• Punto di fusione: 189-193 °C
• Stringa SMILE: Cc1cc(C)cc(c1)P(c2cc(C)cc(C)c2)c3ccc4ccccc4c3-c5c(ccc6ccccc56)P(c7cc(C)cc(C)c7)c8cc(C)cc(C)c8
• InChI: 1S/C52H48P2/c1-33-21-34(2)26-43(25-33)53(44-27-35(3)22-36(4)28-44)49-19-17-41-13-9-11-15-47(41)51(49)52-48-16-12-10-14-42(48)18-20-50(52)54(45-29-37(5)23-38(6)30-45)46-31-39(7)24-40(8)32-46/h9-32H,1-8H3; MXGXXBYVDMVJAO-UHFFFAOYSA-N

Descrizione

Applicazioni

Takasago Ligands and Complexes for Asymmetric Reactions

Catalyst for:

• Asymmetric hydrogenation of benzophenone
• Regio- and stereoselective preparation of axially chiral arylnaphthalene derivatives via rhodium-catalyzed [2+2+2] cycloaddition of diynes with naphthalenepropynoic acid derivatives in the presence of chiral biaryl bisphosphine ligands
• Regiodivergent rhodium-catalyzed [(2+2)+2] carbocyclization of 1,6-enynes with Me propiolates
• Ligand controlled regioselective and stereoselective desymmetrizing rhodium-catalyzed allylic arylation of meso cyclopentene dicarbonates with arylboronic acids to form regioisomeric arylcyclopentenols
• Platinum(II) complex-catalyzed enantioselective aldol reaction with ketene silyl acetals in DMF at room temperature
• Stereoselective preparation of chiral N,O-biaryls via Rh-catalyzed [2+2+2] cycloaddition of conjugate ynamides with diynes

Note legali

Sold in collaboration with Takasago for research purposes only.

Informazioni sulla sicurezza

• Codice della classe di stoccaggio: 11 - Combustible Solids
• Classe di pericolosità dell'acqua (WGK): WGK 3
• Punto d’infiammabilità (°F): Not applicable
• Punto d’infiammabilità (°C): Not applicable
• Dispositivi di protezione individuale: Eyeshields, Gloves, type N95 (US)