4-(Trifluoromethoxy)aniline

Standard for GC, ≥99.9%(GC)

Reagent Code: #238131
fingerprint
CAS Number 461-82-5

science Other reagents with same CAS 461-82-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 177.12 g/mol
Formula C₇H₆F₃NO
badge Registry Numbers
EC Number 207-317-5
MDL Number MFCD00041314
thermostat Physical Properties
Boiling Point 73-75 °C/10 mm Hg(lit.)
inventory_2 Storage & Handling
Density 1.32 g/mL at 20 °C(lit.)
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the production of herbicides and fungicides. Its trifluoromethoxy group enhances lipophilicity and metabolic stability, making it valuable in designing bioactive molecules. Also employed in the development of dyes and specialty polymers due to its electron-withdrawing properties and chemical durability. Commonly utilized in research for constructing complex organic compounds through diazotization and coupling reactions.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,280.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
4-(Trifluoromethoxy)aniline
No image available

Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the production of herbicides and fungicides. Its trifluoromethoxy group enhances lipophilicity and metabolic stability, making it valuable in designing bioactive molecules. Also employed in the development of dyes and specialty polymers due to its electron-withdrawing properties and chemical durability. Commonly utilized in research for constructing complex organic compounds through diazotization and couplin

Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the production of herbicides and fungicides. Its trifluoromethoxy group enhances lipophilicity and metabolic stability, making it valuable in designing bioactive molecules. Also employed in the development of dyes and specialty polymers due to its electron-withdrawing properties and chemical durability. Commonly utilized in research for constructing complex organic compounds through diazotization and coupling reactions.

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...