SPhos Pd G2

• CAS: 1375325-64-6
• Catalog Number: ACM1375325646-1
• Category: Palladium series catalysts
• Molecular Weight: 719.61
• Molecular Formula: C38H44ClNO2PPd
• Synonyms: Chloro(2-dicyclohexylphosphino-2',6'-dimethoxy-1,1'-biphenyl)[2-(2'-amino-1,1'-biphenyl)]palladium(II)
• Melting Point: 218 °C
• Appearance: Powder
• Application: Palladium precatalyst for Suzuki-Miyaura coupling reactions.
• MDL Number: MFCD20264897

Custom Q&A

What is the molecular weight of SPhos Pd G2?

The molecular weight of SPhos Pd G2 is 720.63.

What are the synonyms for SPhos Pd G2?

Some synonyms for SPhos Pd G2 include 2nd Generation SPhos Precatalyst, RK1001022, and Chloro(2-dicyclohexylphosphino-2',6'-dimethoxy-1,1'-biphenyl)(2'-amino-1,1'-biphenyl-2-yl)palladium(II).

What is the melting point of SPhos Pd G2?

The melting point of SPhos Pd G2 is 218°C.

What color is SPhos Pd G2?

SPhos Pd G2 is white in color.

What are the reactions that SPhos Pd G2 is used for?

SPhos Pd G2 is used as a palladium precatalyst for Suzuki-Miyaura coupling reactions.

What improvements were made in the second generation (G2) of SPhos Pd?

In the second generation (G2) of SPhos Pd, the phenethylamine based backbone of the (G1) complex is substituted with a biphenyl-based ligand, allowing for the creation of the active palladium species at room temperature with weak phosphate or carbonate bases.

What is the form of SPhos Pd G2?

SPhos Pd G2 is in powder form.

What is the InChIKey of SPhos Pd G2?

The InChIKey of SPhos Pd G2 is PYMQIHHZINPLDV-UHFFFAOYSA-N.

What is the general description of SPhos Pd G2?

The general description of SPhos Pd G2 indicates that it is remarkably adept at achieving a variety of Suzuki-Miyaura couplings among other cross-coupling reactions.

What are some of the specific uses of SPhos Pd G2?

Some specific uses of SPhos Pd G2 include its application in the self-arylation of 1-alkyl-3-bromo-2-phenyl-2,1-borazaronaphthalenes, Suzuki-Miyaura coupling of [Ru(bpy)2]+ with 4-carboxyphenylboronic acid, and Suzuki-Miyaura coupling of β-borylated porphyrins with 2-iodoaniline.