N-(2-Chloro-6-fluoro-3-nitrophenyl)acetamide

≥95%

Reagent Code: #218166
fingerprint
CAS Number 218796-15-7

science Other reagents with same CAS 218796-15-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 232.60 g/mol
Formula C₈H₆ClFN₂O₃
badge Registry Numbers
MDL Number MFCD00275692
inventory_2 Storage & Handling
Storage Room temperature, dry seal

description Product Description

Used as an intermediate in the synthesis of fluorinated pharmaceuticals and agrochemicals. Its nitro and halogen groups allow further transformations, such as reduction of the nitro group to an amine for use in coupling reactions. Commonly employed in the development of herbicides and antimicrobial agents due to its electron-withdrawing substituents that enhance bioactivity. Also utilized in research for preparing heterocyclic compounds through cyclization reactions.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿700.00
inventory 250mg
10-20 days ฿1,730.00
inventory 1g
10-20 days ฿6,870.00
inventory 5g
10-20 days ฿34,290.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
N-(2-Chloro-6-fluoro-3-nitrophenyl)acetamide
No image available

Used as an intermediate in the synthesis of fluorinated pharmaceuticals and agrochemicals. Its nitro and halogen groups allow further transformations, such as reduction of the nitro group to an amine for use in coupling reactions. Commonly employed in the development of herbicides and antimicrobial agents due to its electron-withdrawing substituents that enhance bioactivity. Also utilized in research for preparing heterocyclic compounds through cyclization reactions.

Used as an intermediate in the synthesis of fluorinated pharmaceuticals and agrochemicals. Its nitro and halogen groups allow further transformations, such as reduction of the nitro group to an amine for use in coupling reactions. Commonly employed in the development of herbicides and antimicrobial agents due to its electron-withdrawing substituents that enhance bioactivity. Also utilized in research for preparing heterocyclic compounds through cyclization 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...