(3aR,8aS)-2-(Pyridin-2-ylmethyl)-8,8a-dihydro-3aH-indeno[1,2-d]oxazole

97%

Reagent Code: #231825
fingerprint
CAS Number 2828433-53-8

science Other reagents with same CAS 2828433-53-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 250.3 g/mol
Formula C₁₆H₁₄N₂O
inventory_2 Storage & Handling
Storage 2-8°C, Sealed, Dry, Light-proof, Inert Gas

description Product Description

Used in pharmaceutical research as a chiral intermediate for synthesizing bioactive molecules, particularly in the development of central nervous system agents. Its rigid polycyclic structure and stereochemistry make it valuable in optimizing drug selectivity and metabolic stability. Commonly employed in asymmetric synthesis and catalysis due to its ability to induce high enantioselectivity. Also explored in the design of enzyme inhibitors where nitrogen-oxygen heterocycles enhance target binding.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,220.00
inventory 250mg
10-20 days ฿19,060.00
inventory 1g
10-20 days ฿55,060.00
(3aR,8aS)-2-(Pyridin-2-ylmethyl)-8,8a-dihydro-3aH-indeno[1,2-d]oxazole
No image available

Used in pharmaceutical research as a chiral intermediate for synthesizing bioactive molecules, particularly in the development of central nervous system agents. Its rigid polycyclic structure and stereochemistry make it valuable in optimizing drug selectivity and metabolic stability. Commonly employed in asymmetric synthesis and catalysis due to its ability to induce high enantioselectivity. Also explored in the design of enzyme inhibitors where nitrogen-oxygen heterocycles enhance target binding.

Used in pharmaceutical research as a chiral intermediate for synthesizing bioactive molecules, particularly in the development of central nervous system agents. Its rigid polycyclic structure and stereochemistry make it valuable in optimizing drug selectivity and metabolic stability. Commonly employed in asymmetric synthesis and catalysis due to its ability to induce high enantioselectivity. Also explored in the design of enzyme inhibitors where nitrogen-oxygen heterocycles enhance target binding.

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...