PCy3 Pd G2
ALDRICH/756741 - 95%
Synonym: Chloro[(tricyclohexylphosphine)
CAS Number: 1353658-81-7
Empirical Formula (Hill Notation): C30H43ClNPPd
Molecular Weight: 590.52
MDL Number: MFCD21363051
Linear Formula: C30H43ClNPPd
Product Type: Chemical
| assay | 95% |
| feature | generation 2 |
| form | solid |
| functional group | phosphine |
| InChI | 1S/C18H33P.C12H10N.ClH.Pd |
| InChI key | CYJRABDADOSMKA-UHFFFAOYSA |
| mp | 244-246 °C |
| Quality Level | 100 ![]() |
| reaction suitability | core: palladium |
| reaction type: Buchwald-Hartwig Cross Coupling Reaction | |
| reaction type: C-H Activation | |
| reaction type: Heck Reaction | |
| reaction type: Hiyama Coupling | |
| reaction type: Negishi Coupling | |
| reaction type: Sonogashira Coupling | |
| reaction type: Stille Coupling | |
| reaction type: Suzuki-Miyaura Coupling | |
| reagent type: catalyst reaction type: Cross Couplings |
|
| SMILES string | NC1=C(C2=C([Pd]Cl)C=CC=C2 |
| Application: | PCy3 Pd G2 is a monophosphine-coordinated 2-phenylaniline-based palladacycle complex that can be used as a precatalyst: • To prepare diarylmethanes by Suzuki cross-coupling reaction with heterocyclic-chloromethyl derivatives with aryl/heteroaryl boronic acids. • To synthesize poly(arylene)s by the Suzuki cross-coupling polymerization reaction between aryl dihalides and aryldiboronic acids. • In the C-H bond functionalization reactions. |
| Packaging: | 1, 5 g in glass bottle |
| Hazard Codes | Xi |
| Risk Statements | 36/37/38 |
| Safety Statements | 26 |
| RIDADR | NONH for all modes of transport |
| WGK Germany | WGK 3 |
| Flash Point(F) | Not applicable |
| Flash Point(C) | Not applicable |
| Purity | 95% |
| mp | 244-246 °C |
| UNSPSC | 12161600 |

