N-(3-[2-Chloro-5-(trifluoromethyl)pyrimidin-4-yl]aminophenyl)prop-2-enamide

98%

Reagent Code: #215982
fingerprint
CAS Number 1374507-25-1

science Other reagents with same CAS 1374507-25-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 342.7 g/mol
Formula C₁₄H₁₀ClF₃N₄O
badge Registry Numbers
MDL Number MFCD28965167
inventory_2 Storage & Handling
Storage -20°C, Sealed, Dry

description Product Description

Used as a key intermediate in the synthesis of agrochemicals, particularly herbicides and insecticides, due to its ability to disrupt specific enzyme pathways in pests and weeds. Its structure enables effective binding to target sites in pest organisms, enhancing the potency and selectivity of the final active ingredient. Also explored in pharmaceutical research for its potential in developing kinase inhibitor-based therapeutics. The presence of the trifluoromethyl and chloropyrimidine groups contributes to improved metabolic stability and bioavailability in active compounds.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿22,140.00
N-(3-[2-Chloro-5-(trifluoromethyl)pyrimidin-4-yl]aminophenyl)prop-2-enamide
No image available

Used as a key intermediate in the synthesis of agrochemicals, particularly herbicides and insecticides, due to its ability to disrupt specific enzyme pathways in pests and weeds. Its structure enables effective binding to target sites in pest organisms, enhancing the potency and selectivity of the final active ingredient. Also explored in pharmaceutical research for its potential in developing kinase inhibitor-based therapeutics. The presence of the trifluoromethyl and chloropyrimidine groups contributes

Used as a key intermediate in the synthesis of agrochemicals, particularly herbicides and insecticides, due to its ability to disrupt specific enzyme pathways in pests and weeds. Its structure enables effective binding to target sites in pest organisms, enhancing the potency and selectivity of the final active ingredient. Also explored in pharmaceutical research for its potential in developing kinase inhibitor-based therapeutics. The presence of the trifluoromethyl and chloropyrimidine groups contributes to improved metabolic stability and bioavailability in active 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...