Basic information Reaction Safety Supplier Related

RuPhos Pd G1 Methyl t--Butyl Ether Adduct

Basic information Reaction Safety Supplier Related

RuPhos Pd G1 Methyl t--Butyl Ether Adduct Basic information

Product Name:
RuPhos Pd G1 Methyl t--Butyl Ether Adduct
Synonyms:
  • Chloro(2-dicyclohexylphosphino-2',6'-di-i-propoxy-1,1'-biphenyl)[2-(2-aminoethylphenyl)]palladium(II), methyl-t-butylether adduct, min. 98%
  • Chloro(2-dicyclohexylphosphino-2',6'-di-i-propoxy-1,1'-biphenyl)[2-(2-aminoethylphenyl)]palladium(II), methyl-t-butylether adduct, min. 98% [RuPhos Palladacycle]
  • (2-Dicyclohexylphosphino-2′,6′-diisopropyl-1,1′-biphenyl)[2-(2-aminoethyl)phenyl)]palladium(II)
  • Chloro(2-dicyclohexylphosphino-2',6'-di-i-propoxy-1,1'-biphenyl)[2-(2-aMinoethylphenyl)]palladiuM(II),Methyl-t-butyletheradduct,Min.98%
  • Chloro(2-dicyclohexylphosphino-2',6'-diisopropoxy-1,1-biphenyl)[2-(2-aminoethylphenyl)]palladium(II)
  • Chloro(2-dicyclohexylphosphino-2',6'-di-i-propoxy-1,1'-biphenyl)[2-(2-aMinoethylphenyl)]palladiuM(II), Methyl-t-butylether adduct,98% RuPhos Palladacycle
  • Chloro-(2-Dicyclohexylphosphino-2′,6′-diisopropoxy-1,1′-biphenyl)[2-(2-aminoethyl)phenyl]palladium(II) - methyl-t-butyl ether adduct (RuPhos Precatalyst 1st Gen)
  • Chloro(2-dicyclohexylphosphino-2',6'-di-i-propoxy-1,1'-biphenyl)[2-(2-aminoethylphenyl)]palladium(II), methyl-t-butylether adduct, min. 98% [RuPhos Palladacycle Gen. 1]
CAS:
1028206-60-1
MF:
C43H65ClNO3PPd
MW:
816.827861
Product Categories:
  • Buchwald Ligands&Precatalysts
  • Buchwald Precatalysts Series
  • Pd
Mol File:
1028206-60-1.mol
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RuPhos Pd G1 Methyl t--Butyl Ether Adduct Chemical Properties

storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
form 
Powder
color 
off-white to beige
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RuPhos Pd G1 Methyl t--Butyl Ether Adduct Usage And Synthesis

Reaction

  1. Catalyst used in the thermal dehydrogenative Diels-Alder reaction of styrenes.
  2. Catalyst used for the CN-cross coupling reactions of 3-halo-2-aminopyridines.
  3. Catalyst used for the domino reaction of two aryl iodides, involving two C-H functionizations.

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