4-Chloro-2-(trifluoromethyl)aniline hydrochloride

97%

Reagent Code: #131949
fingerprint
CAS Number 648415-76-3

science Other reagents with same CAS 648415-76-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 232.03 g/mol
Formula C₇H₆Cl₂F₃N
inventory_2 Storage & Handling
Storage Room temperature, seal, inert gas

description Product Description

Used as a key intermediate in the synthesis of agricultural chemicals, particularly herbicides and fungicides. Its structure supports the development of active ingredients that target specific plant enzymes, enhancing selectivity and effectiveness. Also employed in the production of specialty dyes and pharmaceuticals due to its reactive amine group and stability under various reaction conditions. The presence of chlorine and trifluoromethyl groups contributes to improved lipophilicity and bioavailability in final products.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,260.00
inventory 1g
10-20 days ฿3,400.00
inventory 5g
10-20 days ฿12,860.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
4-Chloro-2-(trifluoromethyl)aniline hydrochloride
No image available
Used as a key intermediate in the synthesis of agricultural chemicals, particularly herbicides and fungicides. Its structure supports the development of active ingredients that target specific plant enzymes, enhancing selectivity and effectiveness. Also employed in the production of specialty dyes and pharmaceuticals due to its reactive amine group and stability under various reaction conditions. The presence of chlorine and trifluoromethyl groups contributes to improved lipophilicity and bioavailability in
Used as a key intermediate in the synthesis of agricultural chemicals, particularly herbicides and fungicides. Its structure supports the development of active ingredients that target specific plant enzymes, enhancing selectivity and effectiveness. Also employed in the production of specialty dyes and pharmaceuticals due to its reactive amine group and stability under various reaction conditions. The presence of chlorine and trifluoromethyl groups contributes to improved lipophilicity and bioavailability in final products.
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...