Ethyl 2,4,5-trifluoro-3-hydroxybenzoate

97%

Reagent Code: #180621
fingerprint
CAS Number 128426-84-6

science Other reagents with same CAS 128426-84-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 220.15 g/mol
Formula C₉H₇F₃O₃
thermostat Physical Properties
Boiling Point 291.0±40.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.421±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of fluorinated pharmaceuticals, particularly in the development of anti-inflammatory and central nervous system agents. Its trifluorinated aromatic structure enhances metabolic stability and bioavailability in drug candidates. Also employed in the preparation of specialty agrochemicals, where the fluorine substituents improve lipophilicity and target binding. Commonly utilized in research settings for building blocks in medicinal chemistry due to its reactive hydroxyl and ester functional groups, allowing for further derivatization.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,580.00
inventory 500mg
10-20 days ฿5,740.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
Ethyl 2,4,5-trifluoro-3-hydroxybenzoate
No image available

Used as an intermediate in the synthesis of fluorinated pharmaceuticals, particularly in the development of anti-inflammatory and central nervous system agents. Its trifluorinated aromatic structure enhances metabolic stability and bioavailability in drug candidates. Also employed in the preparation of specialty agrochemicals, where the fluorine substituents improve lipophilicity and target binding. Commonly utilized in research settings for building blocks in medicinal chemistry due to its reactive hydr

Used as an intermediate in the synthesis of fluorinated pharmaceuticals, particularly in the development of anti-inflammatory and central nervous system agents. Its trifluorinated aromatic structure enhances metabolic stability and bioavailability in drug candidates. Also employed in the preparation of specialty agrochemicals, where the fluorine substituents improve lipophilicity and target binding. Commonly utilized in research settings for building blocks in medicinal chemistry due to its reactive hydroxyl and ester functional groups, allowing for further derivatization.

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...