Basic information Reaction Safety Supplier Related

N-[2-(di-1-adamantylphosphino) phenyl]morpholine,98% Mor-DalPhos

Basic information Reaction Safety Supplier Related

N-[2-(di-1-adamantylphosphino) phenyl]morpholine,98% Mor-DalPhos Basic information

Product Name:
N-[2-(di-1-adamantylphosphino) phenyl]morpholine,98% Mor-DalPhos
Synonyms:
  • N-[2-(di-1-adamantylphosphino) phenyl]morpholine,98% Mor-DalPhos
  • 98% Mor-DalPhos
  • N-[2-(di-1-adaMantylphosphino)phenyl]Morpholine
  • N-[2-(di-1-adaMantylphosphino)phenyl]Morpholine Mor-DalPhos
  • Bis(adamant-1-yl)(2-morpholinophenyl)phosphine
  • Di(1-adamantyl)-2-morpholinophenylphosphine
  • 4-(2-(di(adamantan-1-yl)phosphanyl)phenyl)morpholine
  • Bis(1-adamantyl)(2-morpholinophenyl)-phosphine (Mor-DalPhos)
CAS:
1237588-12-3
MF:
C30H42NOP
MW:
463.63
Product Categories:
  • Achiral Phosphine
  • Aryl Phosphine
  • organophosphine ligand
Mol File:
1237588-12-3.mol
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N-[2-(di-1-adamantylphosphino) phenyl]morpholine,98% Mor-DalPhos Chemical Properties

Melting point:
219-224°C
storage temp. 
2-8°C
form 
crystal
pka
4.75±0.40(Predicted)
color 
white to yellow
Sensitive 
air sensitive
CAS DataBase Reference
1237588-12-3
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26
WGK Germany 
3
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N-[2-(di-1-adamantylphosphino) phenyl]morpholine,98% Mor-DalPhos Usage And Synthesis

Reaction

  1. P-N-ligand for use in the Pd-catalyzed cross-coupling of ammonia and hydrazine. Ref. (2) with a diverse range of sterically hindered, unbiased aryl chlorides. Low catalyst loading and mild conditions. Ref (5) with diamines in a chemoselective arylation process. Ref (6) with solvent-free or aqueous conditions.
  2. P-N-ligand for the gold-catalyzed stereoselective hydroamination of internal alkynes with dialkylamines to afford E-amines.
  3. P-N-ligand for use in the Pd-catalyzed for mono-α-arylation of ketones employing aryl chlorides, bromides, iodides, mesylates (Ref. 7) and tosylates.

Uses

Mor-DalPhos is a versatile and efficient green catalytic system for Buchwald-Hartwig cross-coupling reaction of aryl bromides or chlorides with a large set amines, amides, ureas, and carbamates.

Uses

MorDalphos is an electronically rich, sterically hindered P,N-based ancillary ligand developed by the Stradiotto group that can be used in the Buchwald-Hartwig Amination reaction, alkyne hydroamination and monoarylation of compounds such as ammonia, hydrazine, and acetone.

N-[2-(di-1-adamantylphosphino) phenyl]morpholine,98% Mor-DalPhosSupplier

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N-[2-(di-1-adamantylphosphino) phenyl]morpholine,98% Mor-DalPhos(1237588-12-3)Related Product Information