5-ethyl-3-(trifluoromethyl)-1H-Pyrazole

95%

Reagent Code: #196370
fingerprint
CAS Number 436806-62-1

science Other reagents with same CAS 436806-62-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 164.13 g/mol
Formula C₆H₇F₃N₂
badge Registry Numbers
MDL Number MFCD08701188
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of agrochemicals, particularly in the development of herbicides and insecticides. Its structure supports bioactive properties that enhance crop protection by disrupting pest metabolic pathways. Also explored in pharmaceutical research for anti-inflammatory and antimicrobial agents due to its ability to interact with biological targets through hydrogen bonding and lipophilic interactions. The trifluoromethyl group improves metabolic stability, making it valuable in designing long-acting compounds.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿4,240.00
500mg
10-20 days ฿11,720.00
5-ethyl-3-(trifluoromethyl)-1H-Pyrazole
No image available

Used as a key intermediate in the synthesis of agrochemicals, particularly in the development of herbicides and insecticides. Its structure supports bioactive properties that enhance crop protection by disrupting pest metabolic pathways. Also explored in pharmaceutical research for anti-inflammatory and antimicrobial agents due to its ability to interact with biological targets through hydrogen bonding and lipophilic interactions. The trifluoromethyl group improves metabolic stability, making it valuable

Used as a key intermediate in the synthesis of agrochemicals, particularly in the development of herbicides and insecticides. Its structure supports bioactive properties that enhance crop protection by disrupting pest metabolic pathways. Also explored in pharmaceutical research for anti-inflammatory and antimicrobial agents due to its ability to interact with biological targets through hydrogen bonding and lipophilic interactions. The trifluoromethyl group improves metabolic stability, making it valuable in designing long-acting 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...