Ethyl 2-(3,4,5 trifluoroanilino) nicotinate

Reagent Code: #181198
fingerprint
CAS Number 1350515-51-3

science Other reagents with same CAS 1350515-51-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 296.249 g/mol
Formula C₁₄H₁₁F₃N₂O₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports binding to specific enzyme targets, enhancing selectivity and potency in drug candidates. Also employed in agrochemical research for designing novel pesticides, including herbicides for controlling broadleaf weeds in crops such as corn and soybeans, with improved metabolic stability due to fluorine substitution. Commonly utilized in medicinal chemistry for structure-activity relationship (SAR) studies involving nicotinate derivatives.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿22,800.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
Ethyl 2-(3,4,5 trifluoroanilino) nicotinate
No image available

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports binding to specific enzyme targets, enhancing selectivity and potency in drug candidates. Also employed in agrochemical research for designing novel pesticides, including herbicides for controlling broadleaf weeds in crops such as corn and soybeans, with improved metabolic stability due to fluorine substitution. Commonly utilized in medici

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports binding to specific enzyme targets, enhancing selectivity and potency in drug candidates. Also employed in agrochemical research for designing novel pesticides, including herbicides for controlling broadleaf weeds in crops such as corn and soybeans, with improved metabolic stability due to fluorine substitution. Commonly utilized in medicinal chemistry for structure-activity relationship (SAR) studies involving nicotinate derivatives.

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...