![(SP-4-3)-[[2′,6′-Bis(1-methylethoxy)[1,1′-biphenyl]-2-yl]dicyclohexylphosphine-κP](methanesulfonat…](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fcas-image%2Fthumb-webp%2F353344-sp-4-3-26-bis-1-methylethoxy-11-biphenyl-2-yl-dicyclohexylphosphine-kp-methanesulfonato-ko-2-methylamino-kn-11-biphenyl-2-yl-kc-palladium.webp&w=3840&q=75)
CAS 1599466-85-9
:(SP-4-3)-[[2′,6′-Bis(1-methylethoxy)[1,1′-biphenyl]-2-yl]dicyclohexylphosphine-κP](methanesulfonato-κO)[2′-(methylamino-κN)[1,1′-biphenyl]-2-yl-κC]palladium
Description:
The chemical substance with the name "(SP-4-3)-[[2′,6′-Bis(1-methylethoxy)[1,1′-biphenyl]-2-yl]dicyclohexylphosphine-κP](methanesulfonato-κO)[2′-(methylamino-κN)[1,1′-biphenyl]-2-yl-κC]palladium" and CAS number "1599466-85-9" is a palladium complex that features a chiral phosphine ligand and a methanesulfonate group. This compound is characterized by its coordination of palladium to a bidentate ligand system, which enhances its catalytic properties, particularly in cross-coupling reactions. The presence of bulky substituents, such as dicyclohexylphosphine and methylethoxy groups, contributes to its steric and electronic properties, making it suitable for asymmetric synthesis. Additionally, the methylamino group may influence the solubility and reactivity of the complex. Overall, this compound is of interest in organometallic chemistry and catalysis, particularly in the development of efficient and selective catalytic systems for organic transformations.
Formula:C44H58NO5PPdS
InChI:InChI=1S/C30H43O2P.C13H12N.CH4O3S.Pd/c1-22(2)31-27-19-13-20-28(32-23(3)4)30(27)26-18-11-12-21-29(26)33(24-14-7-5-8-15-24)25-16-9-6-10-17-25;1-14-13-10-6-5-9-12(13)11-7-3-2-4-8-11;1-5(2,3)4;/h11-13,18-25H,5-10,14-17H2,1-4H3;2-7,9-10,14H,1H3;1H3,(H,2,3,4);/q;-1;;+2/p-1
InChI key:InChIKey=SQAROTSTPFXDOK-UHFFFAOYSA-M
SMILES:[P]([Pd+2]1([O-]S(C)(=O)=O)[C-]=2C(C=3C([NH]1C)=CC=CC3)=CC=CC2)(C4=C(C=CC=C4)C5=C(OC(C)C)C=CC=C5OC(C)C)(C6CCCCC6)C7CCCCC7
Synonyms:- RuPhosPdG4
- Palladium, [[2′,6′-bis(1-methylethoxy)[1,1′-biphenyl]-2-yl]dicyclohexylphosphine-κP](methanesulfonato-κO)[2′-(methylamino-κN)[1,1′-biphenyl]-2-yl-κC]-, (SP-4-3)-
- (SP-4-3)-[[2′,6′-Bis(1-methylethoxy)[1,1′-biphenyl]-2-yl]dicyclohexylphosphine-κP](methanesulfonato-κO)[2′-(methylamino-κN)[1,1′-biphenyl]-2-yl-κC]palladium
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Found 5 products.
Methanesulfonato(2-dicyclohexylphosphino-2',6'-di-i-propoxy-1,1'-biphenyl)(2'-methylamino-1,1'-biphenyl-2-yl)palladium(II), min. 98% [RuPhos Palladacycle Gen. 4]
CAS:<p>Methanesulfonato(2-dicyclohexylphosphino-2',6'-di-i-propoxy-1,1'-biphenyl)(2'-methylamino-1,1'-biphenyl-2-yl)palladium(II), min. 98% [RuPhos Palladacycle Gen. 4]</p>Formula:C44H58NO5PPdSPurity:min. 98%Color and Shape:off-white to tan pwdr.Molecular weight:850.40Methanesulfonato(2-Dicyclohexylphosphino-2,6-di-i-Propoxy-1,1-Biphenyl)(2-Methylamino-1,1-Biphenyl-2-yl)Palladium(II)
CAS:Methanesulfonato(2-Dicyclohexylphosphino-2,6-di-i-Propoxy-1,1-Biphenyl)(2-Methylamino-1,1-Biphenyl-2-yl)Palladium(II)Purity:98%Molecular weight:850.39g/molRuPhos Pd G4
CAS:RuPhos Pd G4 is a versatile catalyst used in various chemical reactions. It is commonly used in the synthesis of copolymers, herbicides, and polymers. This catalyst has been proven effective in promoting reactions involving propionate and methanol. Additionally, RuPhos Pd G4 has shown promising results in blood lead analysis and fatty acid synthesis. It has also been utilized in the production of cephalosporins and alkaloids. With its photocatalytic properties, this catalyst can be employed in electrode manufacturing and perfluoroalkyl compound synthesis. Researchers and chemical enthusiasts alike can benefit from using RuPhos Pd G4 for their diverse needs.Formula:C44H58NO5PPdSPurity:Min. 95%Molecular weight:850.39 g/molMethanesulfonato(2-dicyclohexylphosphino-2',6'-di-i-propoxy-1,1'-biphenyl)(2'-methylamino-1,1'-biphenyl-2-yl)palladium(II), min
CAS:Formula:C44H58NO5PPdSPurity:98%Color and Shape:SolidMolecular weight:850.3937810000011
