(R)-tert-Butyl 3,3-difluoro-4-hydroxypiperidine-1-carboxylate

98%

Reagent Code: #231283
fingerprint
CAS Number 1893408-14-4

science Other reagents with same CAS 1893408-14-4

blur_circular Chemical Specifications

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

description Product Description

Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of fluorinated piperidine-containing drugs. Its structure supports enhanced metabolic stability and bioavailability, making it valuable in medicinal chemistry for CNS-targeted therapies and enzyme inhibitors. The presence of the difluoro and hydroxyl groups allows for further functionalization, enabling the construction of complex drug molecules with high stereoselectivity. Commonly employed in the preparation of investigational compounds for diabetes, neurological disorders, and antiviral treatments.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,850.00
inventory 250mg
10-20 days ฿6,260.00
inventory 1g
10-20 days ฿17,610.00
inventory 5g
10-20 days ฿71,890.00
(R)-tert-Butyl 3,3-difluoro-4-hydroxypiperidine-1-carboxylate
No image available

Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of fluorinated piperidine-containing drugs. Its structure supports enhanced metabolic stability and bioavailability, making it valuable in medicinal chemistry for CNS-targeted therapies and enzyme inhibitors. The presence of the difluoro and hydroxyl groups allows for further functionalization, enabling the construction of complex drug molecules with high stereoselectivity. Commonly employed in th

Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of fluorinated piperidine-containing drugs. Its structure supports enhanced metabolic stability and bioavailability, making it valuable in medicinal chemistry for CNS-targeted therapies and enzyme inhibitors. The presence of the difluoro and hydroxyl groups allows for further functionalization, enabling the construction of complex drug molecules with high stereoselectivity. Commonly employed in the preparation of investigational compounds for diabetes, neurological disorders, and antiviral treatments.

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...