3,6-Dichloro-4-(trifluoromethyl)pyridazine

95%

Reagent Code: #179449
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CAS Number 1057672-68-0

science Other reagents with same CAS 1057672-68-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 216.98 g/mol
Formula C₅HCl₂F₃N₂
badge Registry Numbers
MDL Number MFCD08704310
thermostat Physical Properties
Melting Point 45-50 °C
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as an intermediate in the synthesis of agricultural chemicals, particularly in the development of herbicides and plant growth regulators. Its structure supports the design of compounds with selective activity against broadleaf weeds. Also investigated for use in pharmaceutical research due to the bioactive potential of pyridazine derivatives, especially in the development of compounds with antifungal and anti-inflammatory properties. Its chlorine and trifluoromethyl groups enhance stability and influence electron distribution, making it valuable in optimizing the potency and metabolic resistance of active ingredients.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,740.00
inventory 500mg
10-20 days ฿10,420.00

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3,6-Dichloro-4-(trifluoromethyl)pyridazine
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Used as an intermediate in the synthesis of agricultural chemicals, particularly in the development of herbicides and plant growth regulators. Its structure supports the design of compounds with selective activity against broadleaf weeds. Also investigated for use in pharmaceutical research due to the bioactive potential of pyridazine derivatives, especially in the development of compounds with antifungal and anti-inflammatory properties. Its chlorine and trifluoromethyl groups enhance stability and infl

Used as an intermediate in the synthesis of agricultural chemicals, particularly in the development of herbicides and plant growth regulators. Its structure supports the design of compounds with selective activity against broadleaf weeds. Also investigated for use in pharmaceutical research due to the bioactive potential of pyridazine derivatives, especially in the development of compounds with antifungal and anti-inflammatory properties. Its chlorine and trifluoromethyl groups enhance stability and influence electron distribution, making it valuable in optimizing the potency and metabolic resistance of active ingredients.

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