![(SP-4-4)-[2-[2-(Amino-κN)ethyl]phenyl-κC]chloro[dicyclohexyl(2′,6′-dimethoxy[1,1′-biphenyl]-2-yl)p…](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fcas-image%2Fthumb-webp%2F314160-sp-4-4-2-2-amino-kn-ethyl-phenyl-kc-chloro-dicyclohexyl-26-dimethoxy-11-biphenyl-2-yl-phosphine-kp-palladium.webp&w=3840&q=75)
CAS 1028206-58-7: (SP-4-4)-[2-[2-(Amino-κN)ethyl]phenyl-κC]chloro[dicyclohexyl(2′,6′-dimethoxy[1,1′-biphenyl]-2-yl)phosphine-κP]palladium
Formula:C34H45ClNO2PPd
InChI:InChI=1S/C26H35O2P.C8H10N.ClH.Pd/c1-27-23-17-11-18-24(28-2)26(23)22-16-9-10-19-25(22)29(20-12-5-3-6-13-20)21-14-7-4-8-15-21;9-7-6-8-4-2-1-3-5-8;;/h9-11,16-21H,3-8,12-15H2,1-2H3;1-4H,6-7,9H2;1H;/q;-1;;+2/p-1
InChI key:InChIKey=RUWSWVWKRCXWAA-UHFFFAOYSA-M
SMILES:[P](C1=C(C=CC=C1)C2=C(OC)C=CC=C2OC)([Pd+2]3([Cl-])[C-]=4C(CC[NH2]3)=CC=CC4)(C5CCCCC5)C6CCCCC6
Synonyms:- (SP-4-4)-[2-[2-(Amino-κN)ethyl]phenyl-κC]chloro[dicyclohexyl(2′,6′-dimethoxy[1,1′-biphenyl]-2-yl)phosphine-κP]palladium
- Chloro(2-Dicyclohexylphosphino-2',6'-Dimethoxy-1,1'-Biphenyl)[2-(2-Aminoethylphenyl)]Palladium(Ii)
- Chloro(2-dicyclohexylphosphino-2',6'-dimethoxy-1,1'-biphenyl)[2-(2-aminoethylphenyl)]palladium(II)methyl-t-butylether adduct
- Palladium, [2-[2-(amino-κN)ethyl]phenyl-κC]chloro[dicyclohexyl(2',6'-dimethoxy[1,1'-biphenyl]-2-yl)phosphine-κP]-, (SP-4-4)-
- Palladium, [2-[2-(amino-κN)ethyl]phenyl-κC]chloro[dicyclohexyl(2′,6′-dimethoxy[1,1′-biphenyl]-2-yl)phosphine-κP]-, (SP-4-4)-
- SPhos Palladacycle
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Found 5 products.
Chloro(2-dicyclohexylphosphino-2',6'-dimethoxy-1,1'-biphenyl)[2-(2-aminoethylphenyl)]palladium(II) methyl-t-butylether adduct
CAS:Formula:C34H45ClNO2PPdPurity:98%Color and Shape:SolidMolecular weight:672.5734Chloro(2-dicyclohexylphosphino-2',6'-dimethoxy-1,1'-biphenyl)[2-(2-aminoethylphenyl)]palladium(II)
CAS:Controlled ProductApplications Chloro(2-dicyclohexylphosphino-2',6'-dimethoxy-1,1'-biphenyl)[2-(2-aminoethylphenyl)]palladium(II) has been used as catalyst in, the studies of CDK 8/19 inhibitors: Discovery of novel and selective CDK8/19 dual inhibitors and elimination of their CYP3A4 time-dependent inhibition potential; Biaryl Phosphine Based Pd(II) Amido Complexes: The Effect of Ligand Structure on Reductive Elimination References Fujimoto J., et al., Bioorg. Med. Chem.: 25, 3018-3033 (2017); Arrechea P. L., et al., J. Am. Chem. Soc.: 138, 12486-12493 (2016)Formula:C26H35O2P·C8H10N·C5H12O·Cl·PdColor and Shape:NeatMolecular weight:760.721Chloro(2-Dicyclohexylphosphino-2,6-Dimethoxy-1,1-Biphenyl)[2-(2-Aminoethylphenyl)]Palladium(II)
CAS:Chloro(2-Dicyclohexylphosphino-2,6-Dimethoxy-1,1-Biphenyl)[2-(2-Aminoethylphenyl)]Palladium(II)Purity:98%Molecular weight:672.57g/molChloro(2-dicyclohexylphosphino-2',6'-dimethoxy-1,1'-biphenyl)[2-(2-aminoethylphenyl)]palladium(II) methyl-t-butylether adduct, min. 98% [SPhos Palladacycle Gen. 1]
CAS:Chloro(2-dicyclohexylphosphino-2',6'-dimethoxy-1,1'-biphenyl)[2-(2-aminoethylphenyl)]palladium(II) methyl-t-butylether adduct, min. 98% [SPhos Palladacycle Gen. 1]Formula:C34H45ClNO2PPdPurity:min. 98%Color and Shape:white pwdr.Molecular weight:672.57Chloro(2-dicyclohexylphosphino-2',6'-dimethoxy-1,1'-biphenyl)[2-(2-aminoethylphenyl)]palladium(II)
CAS:Controlled ProductChloro(2-dicyclohexylphosphino-2',6'-dimethoxy-1,1'-biphenyl)[2-(2-aminoethylphenyl)]palladium(II) is a palladium complex that has anti-fungal activity. It works by binding to the fungal cell membrane and forming pores in it, which leads to cell death. This drug also inhibits the growth of cancer cells by inhibiting the synthesis of DNA and proteins. Chloro(2-dicyclohexylphosphino-2',6'-dimethoxy-1,1'-biphenyl)[2-(2-aminoethylphenyl)]palladium(II) is metabolized by cytochrome P450 enzymes in mammalian cells, and can be modified by urea derivatives.Formula:C34H45ClNO2PPdPurity:Min. 95%Molecular weight:672.57 g/molRef: 3D-FC75208
Discontinued product