ChemicalBook Product Catalog Chemical Reagents Organic reagents Phosphine ligand (2R)-1-(11bR)-(Dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-yl)-2-Methyl-1,2,3,4-tetrahydroquinoline, 98%

(2R)-1-(11bR)-(Dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-yl)-2-Methyl-1,2,3,4-tetrahydroquinoline, 98%

(2R)-1-(11bR)-(Dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-yl)-2-Methyl-1,2,3,4-tetrahydroquinoline, 98% Basic information
Reaction
Product Name:(2R)-1-(11bR)-(Dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-yl)-2-Methyl-1,2,3,4-tetrahydroquinoline, 98%
Synonyms:(2R)-1-(11bR)-(Dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-yl)-2-Methyl-1,2,3,4-tetrahydroquinoline, 98%;(R,Ra)-Me-THQphos;(2R)-1-(11bR)-Dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosph epin-4-yl-1,2,3,4-tetrahydro-2-methylquinoline;(2R)-1-(11BR)-(DINAPHTHO[2,1-D:1',2'-F][1,3,2]DIOXAPHOSPHEPIN-4-YL)-2-METHYL-1,2,3,4-TETRAHYDROQUINOLINE,98%;(2R)-1-(11bR)-(Dinaphtho[2;(2R)-1-(11bR)-(Dinaphtho[2,1-d;[(2R)-1-((11BR)-DINAPHTHO[2,1-D;1',2'-f][1,3,2]dioxaphosphepin-4-yl)-2-Methyl-1,2,3,4-tetrahydroquinoline, 98%
CAS:1186392-43-7
MF:C30H24NO2P
MW:461.49
EINECS:
Product Categories:
Mol File:1186392-43-7.mol
(2R)-1-(11bR)-(Dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-yl)-2-Methyl-1,2,3,4-tetrahydroquinoline, 98% Structure
(2R)-1-(11bR)-(Dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-yl)-2-Methyl-1,2,3,4-tetrahydroquinoline, 98% Chemical Properties
Melting point 210-212 °C
Boiling point 654.3±48.0 °C(Predicted)
pka1.35±0.40(Predicted)
form Powder
color yellow
Sensitive moisture sensitive
CAS DataBase Reference1186392-43-7
Safety Information
MSDS Information
(2R)-1-(11bR)-(Dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-yl)-2-Methyl-1,2,3,4-tetrahydroquinoline, 98% Usage And Synthesis
Reaction
  1. Chiral ligand used in the iridium-catalyzed formation of a chiral five-membered ring spiroindolenine.
  2. Chiral ligand used in an iridium-catalyzed, enantioselective, allylic alkylation reaction.
  3. Chiral ligand used in the iridium-catalyzed, enantioselective functional group substitution at the α-position of β-ketoesters.
Reactions of 1186392-43-7
(2R)-1-(11bR)-(Dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-yl)-2-Methyl-1,2,3,4-tetrahydroquinoline, 98% Preparation Products And Raw materials
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