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