6-Nitro-7-(trifluoromethyl)imidazo[1,2-a]pyridine

95%

Reagent Code: #133796
fingerprint
CAS Number 2383845-26-7

science Other reagents with same CAS 2383845-26-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 231.13 g/mol
Formula C₈H₄F₃N₃O₂
badge Registry Numbers
MDL Number MFCD29067453
inventory_2 Storage & Handling
Density 1.65±0.1 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders. Its structure supports the development of potent GABA-A receptor modulators, making it valuable in the creation of anxiolytic and anticonvulsant drugs. The electron-withdrawing nitro and trifluoromethyl groups enhance binding affinity and metabolic stability, improving drug efficacy. Also employed in agrochemical research for designing novel pesticides with improved selectivity and environmental safety.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿14,370.00
250mg
10-20 days ฿24,390.00
6-Nitro-7-(trifluoromethyl)imidazo[1,2-a]pyridine
No image available

Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders. Its structure supports the development of potent GABA-A receptor modulators, making it valuable in the creation of anxiolytic and anticonvulsant drugs. The electron-withdrawing nitro and trifluoromethyl groups enhance binding affinity and metabolic stability, improving drug efficacy. Also employed in agrochemical research for designing novel pesticides

Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders. Its structure supports the development of potent GABA-A receptor modulators, making it valuable in the creation of anxiolytic and anticonvulsant drugs. The electron-withdrawing nitro and trifluoromethyl groups enhance binding affinity and metabolic stability, improving drug efficacy. Also employed in agrochemical research for designing novel pesticides with improved selectivity and environmental safety.

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...