AA13999
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
100mg | 98% | in stock | $33.00 | $23.00 | - + | |
250mg | 98% | in stock | $42.00 | $29.00 | - + | |
1g | 98% | in stock | $50.00 | $35.00 | - + | |
25g | 97% | in stock | $928.00 | $649.00 | - + |
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*All prices are in USD.
Catalog Number: | AA13999 |
Chemical Name: | [2-[2-(Amino-κN)ethyl]phenyl-κC][bis(1,1-dimethylethyl)[2',4',6'-tris(1-methylethyl)[1,1'-biphenyl]-2-yl]phosphine]chloropalladium |
CAS Number: | 1142811-12-8 |
Molecular Formula: | C37H55ClNPPd |
Molecular Weight: | 686.6861 |
MDL Number: | MFCD12911909 |
SMILES: | CC(c1cc(cc(c1c1ccccc1P([Pd+2]1([Cl-])[NH2]CCC2=CC=CC=[C-]12)(C(C)(C)C)C(C)(C)C)C(C)C)C(C)C)C |
Complexity: | 658 |
Covalently-Bonded Unit Count: | 3 |
Heavy Atom Count: | 41 |
Hydrogen Bond Acceptor Count: | 2 |
Hydrogen Bond Donor Count: | 1 |
Rotatable Bond Count: | 9 |
The complex Chloro[2-(di-tert-butylphosphino)-2′,4′,6′-triisopropyl-1,1′-biphenyl][2-(2-aminoethyl)phenyl)]palladium(II) plays a crucial role in chemical synthesis as a versatile and efficient catalyst. Its unique structure enables it to facilitate a variety of reactions with high selectivity and efficiency.In organic synthesis, this palladium complex is commonly used in cross-coupling reactions such as the Suzuki-Miyaura coupling, Heck reaction, and Sonogashira coupling. These reactions are essential in the construction of complex organic molecules, making this catalyst particularly valuable in the pharmaceutical and agrochemical industries.Additionally, the complex has shown promising results in carbon-carbon and carbon-heteroatom bond formation, enabling the synthesis of a wide range of functionalized compounds. Its high stability and reactivity make it a preferred choice for chemists seeking to streamline their synthetic processes and achieve optimal yields.Overall, the Chloro[2-(di-tert-butylphosphino)-2′,4′,6′-triisopropyl-1,1′-biphenyl][2-(2-aminoethyl)phenyl)]palladium(II) complex serves as a powerful tool in the hands of synthetic chemists, enabling the efficient synthesis of complex molecules with precision and control.