(3S,4S)-tert-Butyl 3-amino-4-fluoropiperidine-1-carboxylate

97%

Reagent Code: #36784
fingerprint
CAS Number 1290191-71-7

science Other reagents with same CAS 1290191-71-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 218.27 g/mol
Formula C₁₀H₁₉FN₂O₂
badge Registry Numbers
MDL Number MFCD28010923
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in an inert gas

description Product Description

This chemical is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various biologically active compounds. Its structure, featuring both amino and fluoro substituents on the piperidine ring, makes it valuable for developing drug candidates, particularly those targeting central nervous system disorders, cardiovascular diseases, and infectious diseases. The tert-butyl carbamate group serves as a protective group for the amine, allowing for selective reactions during complex molecule synthesis. Its stereochemistry (3S,4S) is crucial for achieving the desired pharmacological activity in chiral drug molecules. Additionally, its fluorine atom enhances the metabolic stability and bioavailability of the final drug products. This compound is often employed in medicinal chemistry research to optimize drug potency, selectivity, and pharmacokinetic properties.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿7,902.00
inventory 1g
10-20 days ฿19,791.00
inventory 100mg
10-20 days ฿4,932.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(3S,4S)-tert-Butyl 3-amino-4-fluoropiperidine-1-carboxylate
No image available
This chemical is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various biologically active compounds. Its structure, featuring both amino and fluoro substituents on the piperidine ring, makes it valuable for developing drug candidates, particularly those targeting central nervous system disorders, cardiovascular diseases, and infectious diseases. The tert-butyl carbamate group serves as a protective group for the amine, allowing for selective reactions during co
This chemical is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various biologically active compounds. Its structure, featuring both amino and fluoro substituents on the piperidine ring, makes it valuable for developing drug candidates, particularly those targeting central nervous system disorders, cardiovascular diseases, and infectious diseases. The tert-butyl carbamate group serves as a protective group for the amine, allowing for selective reactions during complex molecule synthesis. Its stereochemistry (3S,4S) is crucial for achieving the desired pharmacological activity in chiral drug molecules. Additionally, its fluorine atom enhances the metabolic stability and bioavailability of the final drug products. This compound is often employed in medicinal chemistry research to optimize drug potency, selectivity, and pharmacokinetic properties.
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...