(3R,4R)-tert-Butyl3-amino-4-fluoropiperidine-1-carboxylate

97%

Reagent Code: #232027
fingerprint
CAS Number 1932499-00-7

science Other reagents with same CAS 1932499-00-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 218.27 g/mol
Formula C₁₀H₁₉FN₂O₂
badge Registry Numbers
MDL Number MFCD23106310
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of protease inhibitors and antiviral drugs. Its chiral structure with defined stereochemistry makes it valuable for constructing biologically active molecules with high selectivity. Commonly employed in medicinal chemistry for optimizing drug potency and metabolic stability, especially in treatments targeting hepatitis C and other viral infections. The presence of both amine and fluorine functionalities allows for versatile chemical modifications, enhancing binding affinity and pharmacokinetic properties in final drug compounds.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿25,010.00
inventory 250mg
10-20 days ฿46,800.00
$product.analytical_desc - NULL

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(3R,4R)-tert-Butyl3-amino-4-fluoropiperidine-1-carboxylate
No image available

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of protease inhibitors and antiviral drugs. Its chiral structure with defined stereochemistry makes it valuable for constructing biologically active molecules with high selectivity. Commonly employed in medicinal chemistry for optimizing drug potency and metabolic stability, especially in treatments targeting hepatitis C and other viral infections. The presence of both amine and fluorine functionalities

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of protease inhibitors and antiviral drugs. Its chiral structure with defined stereochemistry makes it valuable for constructing biologically active molecules with high selectivity. Commonly employed in medicinal chemistry for optimizing drug potency and metabolic stability, especially in treatments targeting hepatitis C and other viral infections. The presence of both amine and fluorine functionalities allows for versatile chemical modifications, enhancing binding affinity and pharmacokinetic properties in final drug compounds.

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...