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Merck

693022

Sigma-Aldrich

(S)-DM-BINAP

别名:

(S)-(-)-2,2′-双[二(3,5-二甲苯基)膦]-1,1′-联萘, (S)-联萘(3,5-二甲苯基)膦

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About This Item

经验公式(希尔记法):
C52H48P2
分子量:
734.89
MDL號碼:
分類程式碼代碼:
12352005
PubChem物質ID:

形狀

solid

光學活性

[α]/D -172°, 20, c = 1 in chloroform

mp

189-193 °C

SMILES 字串

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

InChI 密鑰

MXGXXBYVDMVJAO-UHFFFAOYSA-N

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應用

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

法律資訊

与 Takasago 联合销售,仅供研究之用。日本注册号2041996

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

Eyeshields, Gloves, type N95 (US)


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分析证书(COA)

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