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(R,R)-DIPAMP

CAS No.
55739-58-7
Chemical Name:
(R,R)-DIPAMP
Synonyms
R)-DIPAMP;(-)-DIPAMP;(R,R)-DIPAMP;(R,R)-Dipamp ,0%;(R,R)-DIPAMP,97%;Ethylenebis(2-methoxyphenylphenylphosphine);Ethylenebis[phenyl(2-methoxyphenyl)phosphine];Ethylenebis[(2-methoxyphenyl)phenylphosphine];(R,R)-Diphenylbis-[(o-anisyl)-methylenephosphine];(1R,2R)-Bis[(2-methoxypheny)phenylphosphino]ethane
CBNumber:
CB0300441
Molecular Formula:
C28H28O2P2
Molecular Weight:
458.48
MDL Number:
MFCD05863546
MOL File:
55739-58-7.mol
Last updated:2023-05-11 17:26:00

(R,R)-DIPAMP Properties

Melting point 102-104 °C
Boiling point 580.2±45.0 °C(Predicted)
alpha -88o (C=1 IN CHLOROFORM)
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
FDA UNII BLJ831OWLW

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335-H413
Precautionary statements  P273-P302+P352-P305+P351+P338
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  37/39-26-36/37
WGK Germany  3
TSCA  No
HS Code  29319090
NFPA 704
1
2 0

(R,R)-DIPAMP Chemical Properties,Uses,Production

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 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.

Uses

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

(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] Ethylenebis[phenyl(2-methoxyphenyl)phosphine] (1R,2R)-Bis[(2-methoxyphenyl)phenylphosphino]ethane,90% (R,R)-1,2-Ethanediylbis[(2-methoxyphenyl)phenylphosphine] (R,R)-Dipamp ,0% (R,R)-DIPAMP,(R,R)-1,2-Bis[(2-methoxyphenyl)(phenylphosphino)]ethane, (R,R)-1,2-Ethanediylbis[(2-methoxyphenyl)phenylphosphine], (R,R)-Ethylenebis[(2-methoxyphenyl)phenylphosphine], [(1R,2R)-()-Bis[( (R,R)-Ethylenebis[(2-methoxyphenyl)phenylphosphine] (R,R)-DIPAMP (-)-DIPAMP (R,R)-(-)-1,2-Bis[(2-Methoxyphenyl)(phenyl)phosphino]ethane,(R,R)-DIPAMP (R,R)-ETHYLENEBIS[(2-METHOXYPHENYL)PHENYLPHOSPHINE] (R,R)-DIPAMP (R,R)-(-)-1,2-BIS[(2-METHOXYPHENYL)(PHENYL)PHOSPHINO]ETHANE 1,2-Bis((R)-(2-Methoxyphenyl)(phenyl)phosphino)ethane (R,R)-(-)-1,2-Bis[(2-methoxyphenyl)(phenyl)phosphino]ethane,98% (R,R)-DIPAMP (1R,2R)-Bis[(2-methoxypheny)phenylphosphino]ethane R)-DIPAMP (R,R)-1,2-Bis[(2-methoxyphenyl)phenylphosphino]ethane> Phosphine, 1,1'-(1,2-ethanediyl)bis[1-(2-methoxyphenyl)-1-phenyl-, (1R,1'R)-rel- (R,R)-DIPAMP,97% 1,2-bis((R)-(2-methoxyphenyl)(phenyl)phosphanyl)ethane 55739-58-7 C6H4OCH3C6H5PCH2CH2PC6H4OCH3C6H5 C28H28O2P2 CH3OC6H4PC6H5CH22 Chiral Catalysts, Ligands, and Reagents Asymmetric Synthesis Privileged Ligands Chiral Phosphine Asymmetric Synthesis Phosphine Ligands Synthetic Organic Chemistry organophosphine ligand