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[ CAS No. 115826-95-4 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 115826-95-4
Chemical Structure| 115826-95-4
Structure of 115826-95-4 * Storage: {[proInfo.prStorage]}
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Product Details of [ 115826-95-4 ]

CAS No. :115826-95-4 MDL No. :MFCD00075254
Formula : C44H32Cl2P2Pd Boiling Point : -
Linear Structure Formula :- InChI Key :VDHAUMFISVWIRX-UHFFFAOYSA-L
M.W : 800.00 Pubchem ID :10919878
Synonyms :

Safety of [ 115826-95-4 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P280-P305+P351+P338 UN#:N/A
Hazard Statements:H302+H312+H332-H315-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 115826-95-4 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 115826-95-4 ]

[ 115826-95-4 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 115826-95-4 ]
  • [ 7732-18-5 ]
  • [ CAS Unavailable ]
  • [ 220336-72-1 ]
YieldReaction ConditionsOperation in experiment
90% In acetone at 20℃; for 5h; 144.c (144c); Silver triflate (3.68 g, 2 eq) was added to a water (1 mL) and acetone (200 mL) solution of PdCl2 [(,S)-BINAP] (5.72 g, 7.15 mmol) from 144b at room temperature. The mixture was stirred for 5 h then filtered through celite. The filtrate was concentrated. The residue was dissolved in CH2Cl2 (20 mL) and ether (20 mL). A yellow solid was formed after the solution was stored overnight. The solid was collected by filtration to give the active catalyst [Pd((6)-BINAP)(H2O)2]2+(OTi)2" (6.84 g, 90%).
  • 2
  • [ 75-09-2 ]
  • [ 115826-95-4 ]
  • [ 2923-28-6 ]
  • [ 75-05-8 ]
  • (1,1'-bis(diphenylphosphino)naphthalene)Pd(acetonitrile)(water) trifluoromethanesulfonate*2(dichloromethane)*0.5(water) [ No CAS ]
YieldReaction ConditionsOperation in experiment
97% In dichloromethane; acetonitrile byproducts: AgCl; N2; add. of acetonitrile soln. of silver salt to dichloromethane soln. of Pd complex, stirring for 5 min at room temp.; filtration, evapn. at room temp., recrystn. from CH2Cl2; elem. anal.;
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