| Identification | Back Directory | [Name]
XPhos Pd G1 | [CAS]
1028206-56-5 | [Synonyms]
XPhos Pd
XPhos Pd G1
XPhos precatalyst
XPhos Palladacycle
[2-(2-AMinoethyl)phenyl](chloro)palladiuM-dicyclohexyl(2',4',6'-triisopropyl-2-biphenylyl)phosphine (1:1)
Chloro(2-dicyclohexylphosphino-2',4',6'-tri-i-propyl-1,1'-biphenyl)[2-(2-aminoethyl)phenyl]palladium(II)
Chloro(2-dicyclohexylphosphino-2′,4′,6′-triisopropyl-1,1′-biphenyl)[2-(2-aminoethyl)phenyl)]palladium(II)
Chloro(2-dicyclohexylphosphino-2',4',6'-tri-i-propyl-1,1'-biphenyl)[2-(2-aminoethyl)phenyl] palladium(II) methyl-t-butylether adduct
Chloro(2-dicyclohexylphosphino-2',4',6'-tri-i-propyl-1,1'-biphenyl)[2-(2-aMinoethyl)phenyl]palladiuM(II)Methyl-t-butyletheradduct,Min.98%
Chloro(2-dicyclohexylphosphino-2',4',6'-tri-i-propyl-1,1'-biphenyl)[2-(2-aminoethyl)phenyl] palladium(II) methyl-t-butylether adduct, min. 98%
Palladium, [2-[2-(amino-KappaN)ethyl]phenyl-KappaC]chloro[dicyclohexyl[2',4',6'-tris(1-methylethyl)[1,1'-biphenyl]-2-yl]phosphine]-, (SP-4-4)-
Chloro(2-dicyclohexylphosphino-2',4',6'-tri-i-propyl-1,1'-biphenyl)[2-(2-aMinoethyl)phenyl] palladiuM(II) Methyl-t-butylether adduct,98% XPhos Palladacycle
Chloro(2-dicyclohexylphosphino-2',4',6'-tri-i-propyl-1,1'-biphenyl)[2-(2-aminoethyl)phenyl] palladium(II) methyl-t-butylether adduct, min. 98% [XPhos Palladacycle]
Chloro(2-dicyclohexylphosphino-2',4',6'-tri-i-propyl-1,1'-biphenyl)[2-(2-aminoethyl)phenyl] palladium(II) methyl-t-butylether adduct, min. 98% [XPhos Palladacycle Gen. 1] | [EINECS(EC#)]
1592732-453-0 | [Molecular Formula]
C41H59ClNPPd | [MDL Number]
MFCD13194128 | [MOL File]
1028206-56-5.mol | [Molecular Weight]
738.77 |
| Chemical Properties | Back Directory | [Melting point ]
205-210°C | [form ]
Powder | [color ]
white | [InChIKey]
WGWWUSKFSLEOKS-UHFFFAOYSA-N | [SMILES]
P(C1CCCCC1)(C1CCCCC1)(C1C=CC=CC=1C1C(=CC(C(C)C)=CC=1C(C)C)C(C)C)[Pd+2]1(NCCC2=CC=CC=[C-]12)[Cl-] | [CAS DataBase Reference]
1028206-56-5 |
| Questions And Answer | Back Directory | [Reaction]
- Catalyst for cross-coupling reactions of electron-deficient anilines with aryl chlorides.
- Catalyst for rapid C-N bond-forming process at low catalyst loading.
- Catalyst for C-N cross-coupling reactions, at or below room temperature.
- Catalyst for the synthesis of tetracyclic indoles via intermolecular α-arylation of ketones.
- Catalyst for the cross-coupling of benzyl chlorides with cyclopropanol-derived ketone homoenolates
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| Hazard Information | Back Directory | [Uses]
XPhos Pd G1 is used as androgen receptor modulator for treatment of disorders including prostate cancer. | [Preparation]
XPhos Pd G1 is an insoluble solid that can be prepared by cross-coupling reactions of imidazole derivatives with dioxane. | [General Description]
Material may contain up to 5% pentane | [reaction suitability]
core: palladium
reaction type: Buchwald-Hartwig Cross Coupling Reaction
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 | [Physiological effects]
XPhos Pd G1 has been shown to have anti-infectious properties against bacteria and viruses including influenza A, respiratory syncytial virus (RSV), human immunodeficiency virus (HIV), and hepatitis B. It also has metabolic effects on the body by reducing levels of pyridine compounds and increasing pyrazolyl concentrations in the blood stream. |
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| Company Name: |
J & K SCIENTIFIC LTD.
|
| Telephone: |
18210857532 18210857532 |
| Website: |
https://www.jkchemical.com |
| Company Name: |
Energy Chemical
|
| Telephone: |
400-0056266 18918157536; |
| Website: |
http://www.energy-chemical.com |
| Company Name: |
Sigma-Aldrich
|
| Telephone: |
021-61415566 800-8193336 |
| Website: |
https://www.sigmaaldrich.cn |
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