Tert-butyl((4-aminobicyclo[2.2.2]Octan-1-yl)methyl)carbamate

98%

Reagent Code: #244371
fingerprint
CAS Number 1638769-02-4

science Other reagents with same CAS 1638769-02-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 254.38 g/mol
Formula C₁₄H₂₆N₂O₂
badge Registry Numbers
MDL Number MFCD27987303
inventory_2 Storage & Handling
Storage 2-8°C, avoiding light

description Product Description

Used as an intermediate in pharmaceutical synthesis, particularly in the development of neuroactive compounds. Its rigid bicyclic structure enhances selectivity and stability in drug candidates targeting central nervous system receptors. Commonly employed in the preparation of serotonin and dopamine modulators due to its favorable stereochemistry and amine-protecting group compatibility. Also utilized in medicinal chemistry for optimizing pharmacokinetic properties such as blood-brain barrier penetration and metabolic resistance.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿25,900.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
Tert-butyl((4-aminobicyclo[2.2.2]Octan-1-yl)methyl)carbamate
No image available

Used as an intermediate in pharmaceutical synthesis, particularly in the development of neuroactive compounds. Its rigid bicyclic structure enhances selectivity and stability in drug candidates targeting central nervous system receptors. Commonly employed in the preparation of serotonin and dopamine modulators due to its favorable stereochemistry and amine-protecting group compatibility. Also utilized in medicinal chemistry for optimizing pharmacokinetic properties such as blood-brain barrier penetration

Used as an intermediate in pharmaceutical synthesis, particularly in the development of neuroactive compounds. Its rigid bicyclic structure enhances selectivity and stability in drug candidates targeting central nervous system receptors. Commonly employed in the preparation of serotonin and dopamine modulators due to its favorable stereochemistry and amine-protecting group compatibility. Also utilized in medicinal chemistry for optimizing pharmacokinetic properties such as blood-brain barrier penetration and metabolic resistance.

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...