2-Chloro-N-[4-(trifluoromethyl)phenyl]acetamide

95%

Reagent Code: #163155
fingerprint
CAS Number 2707-23-5

science Other reagents with same CAS 2707-23-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 237.61 g/mol
Formula C₉H₇ClF₃NO
badge Registry Numbers
MDL Number MFCD00084933
thermostat Physical Properties
Melting Point 158 °C
Boiling Point 333.534 °C(Predicted)
inventory_2 Storage & Handling
Density 1.419±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of anti-inflammatory and analgesic agents. It serves as a building block for preparing substituted anilides and other bioactive molecules. Its electrophilic nature allows for nucleophilic substitution reactions, making it valuable in medicinal chemistry for modifying molecular structures to enhance biological activity. Also employed in the preparation of agrochemicals and functional materials due to its stability and reactivity profile.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿3,130.00
inventory 25g
10-20 days ฿13,040.00
inventory 1g
10-20 days ฿1,360.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
2-Chloro-N-[4-(trifluoromethyl)phenyl]acetamide
No image available

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of anti-inflammatory and analgesic agents. It serves as a building block for preparing substituted anilides and other bioactive molecules. Its electrophilic nature allows for nucleophilic substitution reactions, making it valuable in medicinal chemistry for modifying molecular structures to enhance biological activity. Also employed in the preparation of agrochemicals and functional materials due to its stability

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of anti-inflammatory and analgesic agents. It serves as a building block for preparing substituted anilides and other bioactive molecules. Its electrophilic nature allows for nucleophilic substitution reactions, making it valuable in medicinal chemistry for modifying molecular structures to enhance biological activity. Also employed in the preparation of agrochemicals and functional materials due to its stability and reactivity profile.

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...