()-endo-2-Aminonorbornane

97%

Reagent Code: #69064
fingerprint
CAS Number 121055-07-0

science Other reagents with same CAS 121055-07-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 111.18 g/mol
Formula C₇H₁₃N
thermostat Physical Properties
Boiling Point 160°C
inventory_2 Storage & Handling
Density 0.985g/mL
Storage room temperature, dry

description Product Description

Used as a chiral building block in organic synthesis, particularly in the production of pharmaceuticals. It serves as a key intermediate in the development of drugs targeting the central nervous system due to its rigid bicyclic structure, which can enhance binding affinity to biological targets. Additionally, it is employed in asymmetric catalysis to create enantioselective compounds, which are crucial for producing optically active drugs. Its unique stereochemistry also makes it valuable in material science for designing advanced polymers and ligands.

format_list_bulleted Product Specification

Test Parameter Specification
Purity 96.5
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿14,400.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
()-endo-2-Aminonorbornane
No image available

Used as a chiral building block in organic synthesis, particularly in the production of pharmaceuticals. It serves as a key intermediate in the development of drugs targeting the central nervous system due to its rigid bicyclic structure, which can enhance binding affinity to biological targets. Additionally, it is employed in asymmetric catalysis to create enantioselective compounds, which are crucial for producing optically active drugs. Its unique stereochemistry also makes it valuable in material sci

Used as a chiral building block in organic synthesis, particularly in the production of pharmaceuticals. It serves as a key intermediate in the development of drugs targeting the central nervous system due to its rigid bicyclic structure, which can enhance binding affinity to biological targets. Additionally, it is employed in asymmetric catalysis to create enantioselective compounds, which are crucial for producing optically active drugs. Its unique stereochemistry also makes it valuable in material science for designing advanced polymers and ligands.

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...