rel-(11S,31S)-16,36,37,54-Tetramethoxy-12,32-dimethyl-11,12,13,14,31,32,33,34-octahydro-2,6-dioxa-1(7,1),3(8,1)-diisoquinolina-5(1,3),7(1,4)-dibenzenacyclooctaphane

97%

Reagent Code: #236859
fingerprint
CAS Number 23495-89-8

science Other reagents with same CAS 23495-89-8

blur_circular Chemical Specifications

inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used in advanced organic synthesis as a chiral scaffold for asymmetric catalysis. Its rigid, complex macrocyclic structure with multiple stereogenic centers makes it valuable in the development of enantioselective reactions, particularly in pharmaceutical research where stereochemical control is critical. The compound’s fused isoquinoline and benzenacyclooctaphane framework allows for strong substrate binding and high selectivity in catalytic processes. It has been employed in the synthesis of bioactive natural products and as a template for designing novel catalysts in academic and industrial settings.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,560.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
rel-(11S,31S)-16,36,37,54-Tetramethoxy-12,32-dimethyl-11,12,13,14,31,32,33,34-octahydro-2,6-dioxa-1(7,1),3(8,1)-diisoquinolina-5(1,3),7(1,4)-dibenzenacyclooctaphane
No image available

Used in advanced organic synthesis as a chiral scaffold for asymmetric catalysis. Its rigid, complex macrocyclic structure with multiple stereogenic centers makes it valuable in the development of enantioselective reactions, particularly in pharmaceutical research where stereochemical control is critical. The compound’s fused isoquinoline and benzenacyclooctaphane framework allows for strong substrate binding and high selectivity in catalytic processes. It has been employed in the synthesis of bioactive

Used in advanced organic synthesis as a chiral scaffold for asymmetric catalysis. Its rigid, complex macrocyclic structure with multiple stereogenic centers makes it valuable in the development of enantioselective reactions, particularly in pharmaceutical research where stereochemical control is critical. The compound’s fused isoquinoline and benzenacyclooctaphane framework allows for strong substrate binding and high selectivity in catalytic processes. It has been employed in the synthesis of bioactive natural products and as a template for designing novel catalysts in 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...