N-(3-nitro-4-(trifluoromethyl)phenyl)pivalamide

≥95%

Reagent Code: #215409
fingerprint
CAS Number 1236060-58-4

science Other reagents with same CAS 1236060-58-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 290.24 g/mol
Formula C₁₂H₁₃F₃N₂O₃
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors. Its structure supports binding to specific enzyme active sites, making it valuable in drug discovery for cancer and inflammatory diseases. The electron-withdrawing nitro and trifluoromethyl groups enhance its reactivity and selectivity in coupling reactions. Also employed in agrochemical research for designing bioactive molecules with improved metabolic stability.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,900.00
inventory 250mg
10-20 days ฿9,720.00
inventory 1g
10-20 days ฿28,800.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
N-(3-nitro-4-(trifluoromethyl)phenyl)pivalamide
No image available

Used primarily as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors. Its structure supports binding to specific enzyme active sites, making it valuable in drug discovery for cancer and inflammatory diseases. The electron-withdrawing nitro and trifluoromethyl groups enhance its reactivity and selectivity in coupling reactions. Also employed in agrochemical research for designing bioactive molecules with improved metabolic stability.

Used primarily as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors. Its structure supports binding to specific enzyme active sites, making it valuable in drug discovery for cancer and inflammatory diseases. The electron-withdrawing nitro and trifluoromethyl groups enhance its reactivity and selectivity in coupling reactions. Also employed in agrochemical research for designing bioactive molecules with improved metabolic stability.

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...