Basic information Uses Safety Supplier Related
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(R,R)-DIPAMP

Basic information Uses Safety Supplier Related

(R,R)-DIPAMP Basic information

Product Name:
(R,R)-DIPAMP
Synonyms:
  • (1R,2R)-BIS[(2-METHOXYPHENYL)PHENYLPHOSPHINO]ETHANE
  • [(1R,2R)-(-)-BIS[(2-METHOXYPHENYL)PHENYLPHOSPHINO]ETHANE]
  • (R,R)-(-)-1,2-Bis[(2-methoxyphenyl)(phenyl)phosphino]ethane,98%(-)-DIPAMP
  • (R,R)-(-)-1,2-BIS[2-METHOXYPHENYL)(PHENYL)PHOSPHINO]ETHANE (-)-DIPAMP
  • (R,R)-Diphenylbis-[(o-anisyl)-methylenephosphine]
  • (R,R)-Ethylenebis[(2-methoxyphenyl)phenylphosphine], [(1R,2R)-(-)-Bis[(2-methoxyphenyl)phenylphosphino]ethane], (R,R)-1,2-Ethanediylbis[(2-methoxyphenyl)phenylphosphine], (R,R)-1,2-Bis[(2-methoxyphenyl)(phenylphosphino)]ethane
  • Ethylenebis(2-methoxyphenylphenylphosphine)
  • Ethylenebis[(2-methoxyphenyl)phenylphosphine]
CAS:
55739-58-7
MF:
C28H28O2P2
MW:
458.48
Product Categories:
  • Chiral Phosphine
  • Asymmetric Synthesis
  • Phosphine Ligands
  • Synthetic Organic Chemistry
  • organophosphine ligand
Mol File:
55739-58-7.mol
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(R,R)-DIPAMP Chemical Properties

Melting point:
102-104 °C
alpha 
-88o (C=1 IN CHLOROFORM)
Boiling point:
580.2±45.0 °C(Predicted)
refractive index 
-85 ° (C=1, CHCl3)
form 
Crystalline Powder
color 
White
optical activity
[α]22/D 81°, c = 1 in chloroform
CAS DataBase Reference
55739-58-7
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
37/39-26-36/37
WGK Germany 
3
TSCA 
No
HS Code 
29319090

MSDS

  • Language:English Provider:ACROS
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(R,R)-DIPAMP Usage And Synthesis

Uses

Rhodium DIPAMP catalysts have shown high activity and enantioselectivity in the asymmetric hydrogenation of enamides, enol acetates and olefins.

Chemical Properties

White crystalline powder

Uses

(R,R)-DIPAMP is a reactant used in the synthesis of Rhodium diphosphine trinuclear complexes.

Uses

(R, R)-DIPAMP can be used:

  • As a catalyst in the enantioselective [3+2] cycloaddition of γ-substituted allenoates with β-perfluoroalkyl enones and 3-butynoates with electron-deficient olefins to yield substituted cyclopentenes.
  • To prepare its rhodium metal complexes, which are used as catalysts in asymmetric hydrogenation reactions.

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