Basic information Reaction Safety Supplier Related

(11aR)-(+)-5,6,10,11,12,13-Hexahydro-5-phenyl-4H-diindeno[7,1-cd:17ef]phosphocin, min. 97% (R)-SITCP

Basic information Reaction Safety Supplier Related

(11aR)-(+)-5,6,10,11,12,13-Hexahydro-5-phenyl-4H-diindeno[7,1-cd:17ef]phosphocin, min. 97% (R)-SITCP Basic information

Product Name:
(11aR)-(+)-5,6,10,11,12,13-Hexahydro-5-phenyl-4H-diindeno[7,1-cd:17ef]phosphocin, min. 97% (R)-SITCP
Synonyms:
  • (11aR)-(+)-5,6,10,11,12,13-Hexahydro-5-phenyl-4H-diindeno[7,1-cd:17ef]phosphocin, min. 97% (R)-SITCP
  • 4H-Diindeno[7,1-cd:1',7'-ef]phosphocin,5,6,10,11,12,13-hexahydro-5-phenyl-, (11aR)- (9CI)
  • (R)-diMethylene-[7,7′-(1,1′-spiroindan)]-phenylphospholane
  • (11aR)-5,6,10,11,12,13-Hexahydro-5-phenyl-4H-diindeno[7,1-cd:1',7'-ef]phosphocin
  • (R)-SITCP
  • (R)-dimethylene-\n[7,7′-(1,1′-spiroin\ndan)]-phenylphos\npholane
  • (11aR)-(+)-5,6,10,11,12,13-Hexahydro-5-phenyl-4H-diindeno[7,1-cd
  • 17ef]phosphocin, min. 97% (R)-SITCP
CAS:
856407-37-9
MF:
C25H23P
MW:
354.42
Product Categories:
  • Chiral Phosphine
  • Chiral Spiro Ligand
Mol File:
856407-37-9.mol
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(11aR)-(+)-5,6,10,11,12,13-Hexahydro-5-phenyl-4H-diindeno[7,1-cd:17ef]phosphocin, min. 97% (R)-SITCP Chemical Properties

Melting point:
148-149°C
alpha 
+6° (c 0.5, CH2Cl2)
Boiling point:
505.6±50.0 °C(Predicted)
storage temp. 
-20°C, protect from light, stored under nitrogen
form 
solid
color 
white
Sensitive 
air sensitive
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(11aR)-(+)-5,6,10,11,12,13-Hexahydro-5-phenyl-4H-diindeno[7,1-cd:17ef]phosphocin, min. 97% (R)-SITCP Usage And Synthesis

Reaction

  1. Phosphine-catalyzed intra-and intermolecular gamma-addition of nitrogen nucleophiles to allenoates and alkynoates.
  2. Catalytic asymmetric construction of the tryptanthrin skeleton via enantioselective decarboxylative [4+2] cyclization.
  3. Catalytic, enantioselective carbon-oxygen bond formation – phosphine-catalyzed synthesis of benzylic esters via oxidation of benzylic C-H bonds.
  4. Use of a new spirophosphine to achieve catalytic, enantioselective [4+1] annulations of amines with allenes to generate dihydropyrroles.

(11aR)-(+)-5,6,10,11,12,13-Hexahydro-5-phenyl-4H-diindeno[7,1-cd:17ef]phosphocin, min. 97% (R)-SITCPSupplier

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