2-Dicyclohexylphosp...

2-Dicyclohexylphosphino-2',6'-dimethoxybiphenyl 99% Sphos

2-Dicyclohexylphosphino-2',6'-dimethoxybiphenyl 99% Sphos

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  • Min.Order :1 Gram
  • Purity: 99%min
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Keywords

Sphos 2-Dicyclohexylphosphino-2',6'-dimethoxybiphenyl 99% Sphos

Quick Details

  • Appearance:White Powder
  • Application:SPhos [2-Dicyclohexylphosphino-2′,6′-dimethoxybiphenyl] is an air-stable, electron-rich biaryl phosphine ligand developed by the Buchwald group to enhance the reactivity of palladium catalysis d...
  • PackAge:1KG/Bag or Bottle,25KG per Box or Drum ,180KG,241KG Drum or Customized
  • ProductionCapacity:100|Kilogram|Month
  • Storage:Store in dry, dark and ventilated place and keep sealed when not in use .
  • Transportation:By DHL /Fedex /TNT /EMS /Air /Sea etc.

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Details:

2-Dicyclohexylphosphino-2',6'-dimethoxybiphenyl Basic information
Uses Reactions
Product Name:    2-Dicyclohexylphosphino-2',6'-dimethoxybiphenyl
Synonyms:    98% SPhos;2-Dicyclohexylphosphino-2',6'-diMethoxy-1,1'-biphenyl ,98%;2-Dicyclohexylphosphino-2', 6-diMethoxybihenyl;2-DicyclohexylphosphiNA-2',6'-diMethoxybiphenyl;Dicyclohexyl(2',6'-diMethoxy-[1,1'-biphenyl]-2-yl)phosphine;SPhos 97%;2-Dicyclohexylphosphino-2',6'-diMethoxybiphenyl, 6'-diMethoxybiphenyl;2 - dicyclohexyl phosphine - 2 ', 6 '- diMethoxy - 1, 1' - two PCB
CAS:    657408-07-6
MF:    C26H35O2P
MW:    410.53
EINECS:    613-838-2

 

2-Dicyclohexylphosphino-2',6'-dimethoxybiphenyl Chemical Properties
Melting point     164-166°C
Boiling point     513.3±40.0 °C(Predicted)
storage temp.     Refrigerated.
form     crystal
color     white
Sensitive     Air Sensitive

 

2-Dicyclohexylphosphino-2',6'-dimethoxybiphenyl Usage And Synthesis
Uses    SPhos [2-Dicyclohexylphosphino-2′,6′-dimethoxybiphenyl] is an air-stable, electron-rich biaryl phosphine ligand developed by the Buchwald group to enhance the reactivity of palladium catalysis during cross-coupling reactions. 
SPhos may be used as a ligand in the following processes:
• Palladium catalyzed Suzuki-Miyaura cross-coupling reaction between Boc-protected aminomethyltrifluoroborate and aryl chlorides or hetaryl chlorides to form the corresponding aminomethylarenes.• Palladium catalyzed Suzuki-Miyaura cross-coupling reaction between 4-methyl-substituted piperidinylzinc reagent and different aryl or heteroaryl iodides to form various substituted piperidines.• Intramolecular Suzuki-Miyaura coupling to form the 18-membered macrocyclic ring during the multi-step synthesis of riccardin C.
Utilized in conjunction with palladium to form a highly active catalyst for C-N bond formation.
Highly universal ligand for Suzuki-Miyaura coupling; aryl chlorides, hindered biaryls, heterobiaryls.

Chemical Properties    White solid
Uses    suzuki reaction

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