Basic information Reaction Safety Supplier Related

cataCXium A Pd G3

Basic information Reaction Safety Supplier Related

cataCXium A Pd G3 Basic information

Product Name:
cataCXium A Pd G3
Synonyms:
  • ataCXium A Pd G3
  • cataCXium A Palladacycle Gen. 3
  • Methanesulfonato(diadamantyl-n-butylphosphino)-2'-amino-1,1'-biphenyl-2-yl)palladium(II)
  • METHANESULFONATO(DIADAMANTYL-N-BUTYLPHOSPHINO)-2'-AMINO-1,1'-BIPHENYL-2-YL)PALLADIUM(II)DICHLOROMETHANEADDUCT,MIN.95%[CATACXIUMAPALLADACYCLEGEN.3]
  • Methanesulfonato(diadamantyl-n-butylphosphino)-2'-amino-1,1'-biphenyl-2-yl)palladium(II) dichloromethane adduct, min. 95% [cataCXium(R) A Palladacycle Gen. 3]
  • Methanesulfonato(diadamantyl-n-butylphosphino)-2'-amino-1,1'-biphenyl-2-yl)palladium(II) dichloromethane adduct,[cataCXium A Palladacycle Gen. 3]
  • Methanesulfonato(diadamantyl-n-butylphosphino)-2'-amino-1,1'-biphenyl-2-yl)palladium(II) dichloromethane adduct
  • Methanesulfonato(diadamantyl-n-butylphosphino)-2'-amino-1,1'-biphenyl-2-yl)palladium(II) dichloromethane adduct, min. 95% [cataCXium(R) A Palladacycle Gen. 3] ISO 9001:2015 REACH
CAS:
1651823-59-4
MF:
C37H52NO3PPdS
MW:
728.28
Mol File:
1651823-59-4.mol
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cataCXium A Pd G3 Chemical Properties

Melting point:
196-241 °C (decomposition)
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
form 
Powder
color 
off-white
InChI
InChI=1S/C24H39P.C12H9N.CH4O3S.Pd/c1-2-3-4-25(23-11-17-5-18(12-23)7-19(6-17)13-23)24-14-20-8-21(15-24)10-22(9-20)16-24;13-12-9-5-4-8-11(12)10-6-2-1-3-7-10;1-5(2,3)4;/h17-22H,2-16H2,1H3;1-6,8-9,13H;1H3,(H,2,3,4);/q;-2;;+2
InChIKey
VIYNMTFDXQNMCC-UHFFFAOYSA-N
SMILES
P(C12CC3CC(CC(C3)C1)C2)(C12CC3CC(CC(C3)C1)C2)([Pd+2]1(NC2=CC=CC=C2C2=CC=CC=[C-]12)[O-]S(=O)(=O)C)CCCC
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cataCXium A Pd G3 Usage And Synthesis

Reaction

Precatalyst for the palladium-catalyzed cross-coupling of cesium trifluoroborate salts with aryl halides.

Uses

cataCXium? A Pd G3 is a Buchwald third generation precatalyst that can be used in:

  • Direct ortho-arylation of pyridinecarboxylic acids.
  • Catalyzing Suzuki–Miyaura cross-coupling in the synthesis of 1-heteroaryl-3-azabicyclo[3.1.0]hexanes.
  • Palladium-catalyzed carbonylative carboperfluoroalkylation of alkynes.
  • Suzuki–Miyaura coupling reaction of geminal bis(boryl)cyclopropanes in the synthesis of various gem-disubstituted cyclopropanes.

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