Palladacycle Gen. 3
- CAS NO.：1447963-73-6
- Empirical Formula: C41H54N3O3PPdS
- Molecular Weight: 806.35
- Update Date: 2024-03-18 16:05:02
What is Palladacycle Gen. 3?
Reactions
- Catalyst for the highly selective cross-coupling of secondary alkylzinc reagents with heteroaryl halides
- Catalyst for the completely linear-selective Negishi cross-coupling of allylzinc halides with aryl and vinyl electrophiles
General Description
CPhos Pd G3 is a modified G3 precatalyst (G3′). It has been synthesized by Buchwald and coworkers from second generation (G2) precatalyst by methylation of the amino group present on biphenyl backbone. It is a useful catalyst for various cross-coupling reactions. They are versatile catalysts. They have long life in solution and are readily soluble in various organic solvents. G3- precatalysts have been employed in various C-N bond forming reactions.
Properties of Palladacycle Gen. 3
| Melting point: | 176-178 °C (decomposition) |
| form | Powder |
| color | white to off-white |
Safety information for Palladacycle Gen. 3
Computed Descriptors for Palladacycle Gen. 3
| InChIKey | BYZMMBLECCTRMT-UHFFFAOYSA-N |
| SMILES | P(C1CCCCC1)(C1CCCCC1)(C1C=CC=CC=1C1C(=CC=CC=1N(C)C)N(C)C)[Pd+2]1(NC2=CC=CC=C2C2=CC=CC=[C-]12)[O-]S(=O)(=O)C |
New Products
4-AMINO-TETRAHYDRO-PYRAN-4-CARBOXYLIC ACID HCL 4-Aminotetrahydropyran-4-carbonitrile Hydrochloride (R)-3-Aminobutanenitrile Hydrochloride 3-((Dimethylamino)methyl)-5-methylhexan-2-one oxalate 1,4-Dioxa-8-azaspiro[4.5]decane 5-Bromo-2-nitropyridine 4-(Dimethylamino)tetrahydro-2H-pyran-4-carbonitrile Diclofenac Potassium Ornidazole IP Diclofenac Sodium IP/BP/EP/USP Mefenamic Acid IP/BP/EP/USP Aceclofenac IP/BP/EP Nimesulide BP SODIUM AAS SOLUTION ZINC AAS SOLUTION BUFFER SOLUTION PH 10.0(BORATE) GOOCH CRUCIBLE SINTERED AQUANIL 5 BERYLLIUM AAS SOLUTION SODIUM METHYL PARABEN Methylcobalamin (vitamin B12) SODIUM VALPROATE LAMOTRIGINE RacecadotrilRelated products of tetrahydrofuran
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