Methyl 4-amino-5-fluoropicolinate

95%

Reagent Code: #131224
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CAS Number 1260665-42-6

science Other reagents with same CAS 1260665-42-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 170.14 g/mol
Formula C₇H₇FN₂O₂
badge Registry Numbers
MDL Number MFCD18250755
thermostat Physical Properties
Boiling Point 332.8±37.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.339±0.06 g/cm3(Predicted)
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a key intermediate in the synthesis of herbicidal compounds, particularly arylpicolinate-class selective broadleaf herbicides such as florpyrauxifen. Its fluorinated picolinate structure serves as a building block for synthetic auxins that disrupt plant growth regulation by mimicking natural auxin hormones, leading to uncontrolled cell elongation and eventual plant death in susceptible weeds. Commonly employed in agricultural chemistry for developing crop protection agents that offer selectivity for crops like corn and soybeans while minimizing environmental impact. Also utilized in research for creating new fluorinated herbicide analogs with enhanced efficacy and resistance management properties.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿10,700.00
inventory 250mg
10-20 days ฿44,700.00

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Methyl 4-amino-5-fluoropicolinate
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Used as a key intermediate in the synthesis of herbicidal compounds, particularly arylpicolinate-class selective broadleaf herbicides such as florpyrauxifen. Its fluorinated picolinate structure serves as a building block for synthetic auxins that disrupt plant growth regulation by mimicking natural auxin hormones, leading to uncontrolled cell elongation and eventual plant death in susceptible weeds. Commonly employed in agricultural chemistry for developing crop protection agents that offer selectivity

Used as a key intermediate in the synthesis of herbicidal compounds, particularly arylpicolinate-class selective broadleaf herbicides such as florpyrauxifen. Its fluorinated picolinate structure serves as a building block for synthetic auxins that disrupt plant growth regulation by mimicking natural auxin hormones, leading to uncontrolled cell elongation and eventual plant death in susceptible weeds. Commonly employed in agricultural chemistry for developing crop protection agents that offer selectivity for crops like corn and soybeans while minimizing environmental impact. Also utilized in research for creating new fluorinated herbicide analogs with enhanced efficacy and resistance management properties.

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