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

98%, ee 99%

Reagent Code: #39752
fingerprint
CAS Number 1360145-09-0

science Other reagents with same CAS 1360145-09-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 447.464241 g/mol
Formula C₂₉H₂₂NO₂P
badge Registry Numbers
MDL Number MFCD30187350
thermostat Physical Properties
Boiling Point 653.5±48.0 °C
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This chemical is primarily utilized in the field of organic synthesis, particularly as a chiral ligand or catalyst in asymmetric reactions. Its unique structure, featuring a tetrahydroquinoline moiety and a dioxaphosphepine ring, makes it effective in facilitating enantioselective transformations. It is commonly employed in the synthesis of complex organic molecules, including pharmaceuticals and fine chemicals, where high stereochemical control is required. Additionally, it finds application in the development of advanced materials and in research focused on understanding stereochemical outcomes in catalytic processes. Its role in enhancing reaction efficiency and selectivity makes it valuable in both academic and industrial settings.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance White to off-white solid
Purity 97.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100 mg
10-20 days ฿2,950.00
inventory 1 g
10-20 days ฿14,301.00
inventory 250 mg
10-20 days ฿5,290.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
1-[(11bR)-Dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-yl]-1,2,3,4-tetrahydroquinoline
No image available

This chemical is primarily utilized in the field of organic synthesis, particularly as a chiral ligand or catalyst in asymmetric reactions. Its unique structure, featuring a tetrahydroquinoline moiety and a dioxaphosphepine ring, makes it effective in facilitating enantioselective transformations. It is commonly employed in the synthesis of complex organic molecules, including pharmaceuticals and fine chemicals, where high stereochemical control is required. Additionally, it finds application in the deve

This chemical is primarily utilized in the field of organic synthesis, particularly as a chiral ligand or catalyst in asymmetric reactions. Its unique structure, featuring a tetrahydroquinoline moiety and a dioxaphosphepine ring, makes it effective in facilitating enantioselective transformations. It is commonly employed in the synthesis of complex organic molecules, including pharmaceuticals and fine chemicals, where high stereochemical control is required. Additionally, it finds application in the development of advanced materials and in research focused on understanding stereochemical outcomes in catalytic processes. Its role in enhancing reaction efficiency and selectivity makes it valuable in both academic and industrial settings.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...