Methyl 2-bromo-3,5-dichloroisonicotinate

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Reagent Code: #131649
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CAS Number 1807028-93-8

science Other reagents with same CAS 1807028-93-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 284.92 g/mol
Formula C₇H₄BrCl₂NO₂
badge Registry Numbers
MDL Number MFCD26406015
thermostat Physical Properties
Boiling Point 314.3±37.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.773±0.06 g/cm3(Predicted)
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used primarily as a key intermediate in the synthesis of agricultural chemicals, particularly in the development of herbicides and fungicides. Its structure allows for selective modification, making it valuable in creating active ingredients that target specific plant pathogens or unwanted vegetation without significant impact on surrounding crops. Additionally, it serves in the preparation of pharmaceuticals where halogenated pyridine derivatives are required, contributing to the efficacy and stability of certain drug compounds. Its reactivity profile supports coupling reactions and nucleophilic substitutions, enabling its use in various multi-step organic syntheses in both agrochemical and medicinal chemistry research.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,510.00
inventory 250mg
10-20 days ฿5,970.00
inventory 1g
10-20 days ฿16,130.00

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Methyl 2-bromo-3,5-dichloroisonicotinate
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Used primarily as a key intermediate in the synthesis of agricultural chemicals, particularly in the development of herbicides and fungicides. Its structure allows for selective modification, making it valuable in creating active ingredients that target specific plant pathogens or unwanted vegetation without significant impact on surrounding crops. Additionally, it serves in the preparation of pharmaceuticals where halogenated pyridine derivatives are required, contributing to the efficacy and stability

Used primarily as a key intermediate in the synthesis of agricultural chemicals, particularly in the development of herbicides and fungicides. Its structure allows for selective modification, making it valuable in creating active ingredients that target specific plant pathogens or unwanted vegetation without significant impact on surrounding crops. Additionally, it serves in the preparation of pharmaceuticals where halogenated pyridine derivatives are required, contributing to the efficacy and stability of certain drug compounds. Its reactivity profile supports coupling reactions and nucleophilic substitutions, enabling its use in various multi-step organic syntheses in both agrochemical and medicinal chemistry research.

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