ChemicalBook--->CAS DataBase List--->566940-03-2

566940-03-2

566940-03-2 Structure

566940-03-2 Structure
IdentificationBack Directory
[Name]

(R)-(-)-5,5'-Bis[di(3,5-di-t-butyl-4-methoxyphenyl)phosphino]-4,4'-bi-1,3-benzodioxole,min.98%(R)-DTBM-SEGPHOS
[CAS]

566940-03-2
[Synonyms]

DTBM-SEGPHOS
(R)-DTBM-SEGPHOS
(R)-DTBM-SEGPHOS(R)
(R)-(-)-DTBM-SEGPHOS(regR)
(R)-(-)-5,5'-Bis[di(3,5-di-t-butyl-4-Methoxyphenyl)phosphino]-4,4'-bi-1,3-benzodioxole
(R)-()-5,5′-Bis[di(3,5-di-tert-butyl-4-methoxyphenyl)phosphino]-4,4′-bi-1,3-benzodioxole
[(4R)-(4,4′-bi-1,3-benzodioxole)-5,5′-diyl]bis[bis(3,5-di-tert-butyl-4-methoxyphenyl)phosphine]
(R)-(-)-5,5'-Bis[di(3,5-di-t-butyl-4-methoxyphenyl)phosphino]-4,4'-bi-1,3-benzodioxole, min. 98%
(4R)-[4,4'-Bi-1,3-benzodioxole]-5,5'-diylbis[bis[3,5-bis(1,1-dimethylethyl)-4-methoxyphenyl]phosphine
(R)-(-)-5,5'-Bis[di(3,5-di-t-butyl-4-methoxyphenyl)phosphino]-4,4'-bi-1,3-benzodioxole,min.98%(R)-DTBM-SEGPHOS
(R)-(-)-5,5'-Bis[di(3,5-di-t-butyl-4-methoxyphenyl)phosphino]-4,4'-bi-1,3-benzodioxole, min. 98% (R)-(-)-DTBM-SEGPHOS(R)
[(4R)-(4,4μ-bi-1,3-benzodioxole)-5,5μ-diyl]bis[bis(3,5-di-tert-butyl-4-methoxyphenyl)phosphine], (R)-(-)-5,5μ-Bis[di(3,5-di-tert-butyl-4-methoxyphenyl)phosphino]-4,4μ-bi-1,3-benzodioxole
[Molecular Formula]

C74H100O8P2
[MDL Number]

MFCD09753003
[MOL File]

566940-03-2.mol
[Molecular Weight]

1179.55
Chemical PropertiesBack Directory
[Melting point ]

126-128°C
[Boiling point ]

987.3±65.0 °C(Predicted)
[form ]

Powder
[color ]

off-white
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H335-H319
[Precautionary statements ]

P264-P280-P302+P352-P321-P332+P313-P362-P264-P280-P305+P351+P338-P337+P313P
[WGK Germany ]

3
[HS Code ]

2932.99.7000
Questions And AnswerBack Directory
[Reaction]

  1. Rhodium catalyzed chemo-, regio, and entantioselective [2 + 2 + 2] cycloaddition of alkynes with isocyanates.
  2. With copper, enantioselective cross Aldol-type reaction of acetonitrile.
  3. With copper, enantioselective vinylsilane alkenylation of aldehydes.
  4. Gold carbene mediated stereoselective cyclopropanation of propargyl esters.
  5. With copper, enantioselective 1,2-reduction of ketones, and 1,4-reduction of a α,β-usaturated esters.
  6. With copper, catalytic enantioselective Mannich-type reaction.
  7. Enantioselective fluorination of b β-keto esters, tert-butoxycarbonyl lactones and lactmes with Sodeoka's Pd-aqua complex and a fluorinating reagent.
  8. Rh-catalyzed intramolecular olefin or carbonyl hydroacylation.
  9. Pd-catalyzed γ-arylation of β,γ-unsaturated ketones.
  10. Involved in numerous conjugate alkynylation, and ring-opening alkynylation of azabenzonorbornadienes.
  11. Involved in asymmetric hydroamination of bicyclic alkenes/dienes,13a diamination of conjugated dienes,13b and hydroalkoxylation/hydrosulfenylation of allenes.
The actions in the following figures are corresponding to the above ones in sequence. Reactions of 566940-03-2_1
Reactions of 566940-03-2_2
Reactions of 566940-03-2_3
Hazard InformationBack Directory
[Uses]

Catalyst involved in:
  • [3,3]-Sigmatropic rearrangements using cyclopropane probes
  • Asymmetric intramolecular hydroacylation of ketoaldehydes

Reactant involved in:
  • The synthesis of gold-diphosphine complexes for use as catalysts
  • Cycloaddition of allenenes to yield alkylidenecyclobutanes
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