Methyl2-chloro-3-fluoro-6-methylisonicotinate

98%

Reagent Code: #214012
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CAS Number 2090936-83-5

science Other reagents with same CAS 2090936-83-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 203.6 g/mol
Formula C₈H₇ClFNO₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of agrochemicals, particularly in the production of herbicides and insecticides. Its structure allows for selective reactivity in building complex heterocyclic systems, making it valuable in crop protection chemistry. It is also employed in the development of pharmaceuticals where fluorinated pyridine derivatives are needed for enhanced metabolic stability and bioavailability. The compound's chloro and fluoro substituents facilitate cross-coupling reactions, enabling the introduction of various functional groups during multi-step syntheses.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿18,640.00
250mg
10-20 days ฿31,140.00
1g
10-20 days ฿76,440.00
Methyl2-chloro-3-fluoro-6-methylisonicotinate
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Used as a key intermediate in the synthesis of agrochemicals, particularly in the production of herbicides and insecticides. Its structure allows for selective reactivity in building complex heterocyclic systems, making it valuable in crop protection chemistry. It is also employed in the development of pharmaceuticals where fluorinated pyridine derivatives are needed for enhanced metabolic stability and bioavailability. The compound's chloro and fluoro substituents facilitate cross-coupling reactions, en

Used as a key intermediate in the synthesis of agrochemicals, particularly in the production of herbicides and insecticides. Its structure allows for selective reactivity in building complex heterocyclic systems, making it valuable in crop protection chemistry. It is also employed in the development of pharmaceuticals where fluorinated pyridine derivatives are needed for enhanced metabolic stability and bioavailability. The compound's chloro and fluoro substituents facilitate cross-coupling reactions, enabling the introduction of various functional groups during multi-step syntheses.

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