![Dichlorobis[di-tert-butyl(4-dimethylaminophenyl)phosphino]palladium(II)](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fcas-image%2Fthumb-webp%2F308009-dichlorobis-di-tert-butyl-4-dimethylaminophenyl-phosphino-palladium-ii.webp&w=3840&q=75)
CAS 887919-35-9
:Dichlorobis[di-tert-butyl(4-dimethylaminophenyl)phosphino]palladium(II)
Description:
Dichlorobis[di-tert-butyl(4-dimethylaminophenyl)phosphino]palladium(II) is a palladium complex characterized by its coordination of palladium with two bidentate phosphine ligands. The structure features a palladium center coordinated to two chloride ions and two bulky phosphine ligands, which are derived from di-tert-butyl(4-dimethylaminophenyl)phosphine. This complex is notable for its potential applications in catalysis, particularly in cross-coupling reactions, due to the favorable electronic and steric properties imparted by the phosphine ligands. The presence of the dimethylamino group enhances the electron-donating ability of the ligands, which can influence the reactivity of the palladium center. Additionally, the bulky tert-butyl groups provide steric hindrance, which can help stabilize the complex and prevent unwanted side reactions. Overall, this compound exemplifies the versatility of palladium complexes in organic synthesis and materials science, showcasing the interplay between ligand design and catalytic activity.
Formula:C32H56Cl2N2P2Pd
InChI:InChI=1/2C16H28NP.2ClH.Pd/c2*1-15(2,3)18(16(4,5)6)14-11-9-13(10-12-14)17(7)8;;;/h2*9-12H,1-8H3;2*1H;/q;;;;+2/p-2
SMILES:CC(C)(C)P(c1ccc(cc1)N(C)C)C(C)(C)C.CC(C)(C)P(c1ccc(cc1)N(C)C)C(C)(C)C.Cl.Cl.[Pd]
Synonyms:- 4-(Di-tert-butylphosphino)-N,N-dimethylaniline-dichloropalladium (2:1)
- 4-(di-tert-butylphosphanyl)-N,N-dimethylaniline-dichloropalladium (2:1)
- Bis(di-tert-butyl(4-dimethylaminophenyl)phosphine)dichloropalladium(II)
- Dichlorobis(di-tert-butyl-4-dimethylaminophenylphosphine) palladium(II)
- (A-taPhos)2PdCl2
- (AmPhos)2PdCl2
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Found 8 products.
Bis[di-tert-butyl(4-dimethylaminophenyl)phosphine]dichloropalladium(II)
CAS:Formula:C32H56Cl2N2P2PdPurity:>98.0%(T)Color and Shape:Light yellow to Yellow to Orange powder to crystalMolecular weight:708.08Dichlorobis[di-tert-butyl(4-dimethylaminophenyl)phosphine]palladium(II), Pd 15%
CAS:<p>Dichlorobis[di-tert-butyl(4-dimethylaminophenyl)phosphine]palladium(II) is a highly active, air-stable catalyst for Suzuki-Miyaura cross-coupling with aryl halides including 5- and 6-membered heteroaryl chlorides. This Thermo Scientific brand product was originally part of the Alfa Aesar product por</p>Formula:C32H56Cl2N2P2PdMolecular weight:708.08Bis(4-(di-tert-Butylphosphanyl)-N,N-dimethylaniline); palladium chloride
CAS:Formula:C32H56Cl2N2P2PdPurity:98%Color and Shape:SolidMolecular weight:708.0740Bis{bis(tert-butyl)[4-(dimethylamino)phenyl]phosphine}palladium(II) chloride
CAS:Bis{bis(tert-butyl)[4-(dimethylamino)phenyl]phosphine}palladium(II) chlorideFormula:·2C16H28NP·Cl2PdPurity:97%Color and Shape: yellow solidMolecular weight:708.07396g/molPdCl2(amphos)2 (HPMC encapsulated)
CAS:Formula:C32H56Cl2N2P2PdColor and Shape:White to Light yellow capsuleMolecular weight:708.08Bis(4-(di-tert-Butylphosphanyl)-N,N-dimethylaniline)-palladium chloride
CAS:Formula:C32H56Cl2N2P2PdPurity:98%Color and Shape:SolidMolecular weight:708.08Dichlorobis{[4-(N,N-dimethylamino)phenyl]di-t-butylphosphino}palladium(II), min. 98% PdAmphos
CAS:<p>Dichlorobis{[4-(N,N-dimethylamino)phenyl]di-t-butylphosphino}palladium(II), min. 98% PdAmphos</p>Formula:(C16H28NP)2PdCl2Purity:min. 98%Color and Shape:yellow pwdr.Molecular weight:708.07Bis(4-(di-tert-butylphosphino)-N,N-dimethylbenzenamine) palladium dichloride
CAS:Controlled Product<p>Bis(4-(di-tert-butylphosphanyl)-N,N-dimethylaniline) is a boronic acid that has been used as a surfactant in organic chemistry. It is hydrophobic and has hydrogen bonding interactions with other molecules. Bis(4-(di-tert-butylphosphanyl)-N,N-dimethylaniline) is also a proton acceptor and can form stable complexes with metal ions such as palladium chloride. This compound is kinase selective and can be used to inhibit tyrosine kinases by binding to the ATP binding site of the enzyme's kinase domain. The functional groups of this compound are able to undergo cross-coupling reactions with other functional groups that have been activated by a reagent such as palladium chloride. Bis(4-(di-tert-butylphosphanyl)-N,N-dimethylaniline) has been used in high</p>Formula:C32H56Cl2N2P2PdPurity:Min. 95%Color and Shape:PowderMolecular weight:708.07 g/mol
![Bis[di-tert-butyl(4-dimethylaminophenyl)phosphine]dichloropalladium(II)](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2F3B%2Fthumb%2FB6255.jpg&w=3840&q=75)
![Dichlorobis[di-tert-butyl(4-dimethylaminophenyl)phosphine]palladium(II), Pd 15%](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2F02%2Fthumb%2F045511.jpg&w=3840&q=75)
![Bis{bis(tert-butyl)[4-(dimethylamino)phenyl]phosphine}palladium(II) chloride](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2F54%2Fthumb%2FOR17048.jpg&w=3840&q=75)
![Dichlorobis{[4-(N,N-dimethylamino)phenyl]di-t-butylphosphino}palladium(II), min. 98% PdAmphos](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2F08%2Fthumb%2F46-0825.jpg&w=3840&q=75)
