tert-butyl 4-(2-(trifluoromethyl)phenoxy)piperidine-1-carboxylate

≥95%

Reagent Code: #242512
fingerprint
CAS Number 921605-76-7

science Other reagents with same CAS 921605-76-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 345.36 g/mol
Formula C₁₇H₂₂F₃NO₃
thermostat Physical Properties
Boiling Point 394.3±42.0℃(Predicted)
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of central nervous system agents. Its structure supports the creation of bioactive molecules due to the presence of the piperidine ring and the trifluoromethylphenoxy group, which can enhance metabolic stability and binding affinity. Commonly employed in medicinal chemistry for optimizing drug candidates targeting neurological disorders. Also utilized in research settings to explore structure-activity relationships in receptor modulators.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿55,470.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
tert-butyl 4-(2-(trifluoromethyl)phenoxy)piperidine-1-carboxylate
No image available

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of central nervous system agents. Its structure supports the creation of bioactive molecules due to the presence of the piperidine ring and the trifluoromethylphenoxy group, which can enhance metabolic stability and binding affinity. Commonly employed in medicinal chemistry for optimizing drug candidates targeting neurological disorders. Also utilized in research settings to explore structure-activity re

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of central nervous system agents. Its structure supports the creation of bioactive molecules due to the presence of the piperidine ring and the trifluoromethylphenoxy group, which can enhance metabolic stability and binding affinity. Commonly employed in medicinal chemistry for optimizing drug candidates targeting neurological disorders. Also utilized in research settings to explore structure-activity relationships in receptor modulators.

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...