P(t-Bu)3 Pd G4 CAS 1621274-11-0

Introduction：Basic information about P(t-Bu)3 Pd G4 CAS 1621274-11-0, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

P(t-Bu)3 Pd G4 Basic information

• Product Name: P(t-Bu)3 Pd G4
• Synonyms: P(t-Bu)3 Pd G4;Methanesulfonato(tri-t-butylphosphino)(2'-methylamino-1,1'-biphenyl-2-yl)palladium(II),[P(t-Bu)3 Palladacycle Gen. 4];METHANESULFONATO(TRI-T-BUTYLPHOSPHINO)(2'-METHYLAMINO-1,1'-BIPHENYL-2-YL)PALLADIUM(II),98%[P(T-BU)3PALLADACYCLEGEN.4];P(t-Bu)3 Palladacycle Gen. 4;Methanesulfonato(tri-t-butylphosphino)(2'-methylamino-1,1'-biphenyl-2-yl)palladium(II);P(t-Bu)3 Pd G4 / Methanesulfonato(tri-t-butylphosphino)(2'-methylamino-1,1'-biphenyl-2-yl)palladium(II);Methanesulfonato(tri-t-butylphosphino)(2'-methylamino-1,1'-biphenyl-2-yl)palladium(II) ISO 9001：2015 REACH;1-biphenyl-2-yl)palladium(II)
• CAS: 1621274-11-0
• MF: C26H42NO3PPdS
• MW: 586.08
• Mol File: 1621274-11-0.mol

P(t-Bu)3 Pd G4 Chemical Properties

• storage temp.: 2-8°C, protect from light, stored under nitrogen
• form: Powder
• color: tan to yellow
• InChI: InChI=1S/C14H15N.3C4H10P.O3S.Pd/c1-11-7-3-4-8-12(11)13-9-5-6-10-14(13)15-2;3*1-4(2,3)5;1-4(2)3;/h3-10,15H,1-2H3;3*5H,1-3H3;;/q;4*-1;+1
• InChIKey: JBZFBSFINJJLAH-UHFFFAOYSA-N
• SMILES: CC1=CC=CC=C1C1=CC=CC=C1NC.[Pd-2](S([O-])(=O)=O)(PC(C)(C)C)(PC(C)(C)C)PC(C)(C)C
• CAS DataBase Reference: 1621274-11-0

Safety Information

• WGK Germany: WGK 3
• Storage Class: 11 - Combustible Solids

P(t-Bu)3 Pd G4 Usage And Synthesis

Reactions

1. Alternative Pd-catalyzed cross-coupling reaction of s-BuB(OH)2 and 4-chloroanisole.
2. Alternative Pd-catalyzed cross-coupling reaction of secondary alkylboronic acids and aryl chlorides.
3. Alternative Pd-catalyzed cross-coupling reaction of secondary alkyltrifluoroborates and aryl chlorides

Chemical Properties

P(t-Bu)3 Pd G4 is a powder or crystalsis,it's stable, soluble in most organic solvents.

Uses

P(t-Bu)₃ Pd G4 is a powerful ligand for classic cross-coupling reactions combined with the Buchwald Fourth Generation Palladacycle. Bench stable, soluble in most organic solvents.

reaction suitability

reaction type: Buchwald-Hartwig Cross Coupling Reaction
reaction type: Cross Couplings
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