Ethyl 3-bromo-5-methylpicolinate

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Reagent Code: #131269
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CAS Number 1804864-60-5

science Other reagents with same CAS 1804864-60-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 244.09 g/mol
Formula C₉H₁₀BrNO₂
badge Registry Numbers
MDL Number MFCD28746003
thermostat Physical Properties
Boiling Point 306.9±37.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.439±0.06 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and plant growth regulators. Its structure allows for selective functionalization, making it valuable in creating active ingredients that target specific enzymatic pathways in plants. It is also employed in research settings for constructing complex heterocyclic compounds due to the reactivity of the bromo and ester groups, enabling cross-coupling reactions and nucleophilic substitutions. Its role in medicinal chemistry includes building blocks for kinase inhibitors and other bioactive molecules.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,310.00
inventory 250mg
10-20 days ฿19,220.00

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Ethyl 3-bromo-5-methylpicolinate
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Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and plant growth regulators. Its structure allows for selective functionalization, making it valuable in creating active ingredients that target specific enzymatic pathways in plants. It is also employed in research settings for constructing complex heterocyclic compounds due to the reactivity of the bromo and ester groups, enabling cross-coupling reactions and nucleophilic substit
Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and plant growth regulators. Its structure allows for selective functionalization, making it valuable in creating active ingredients that target specific enzymatic pathways in plants. It is also employed in research settings for constructing complex heterocyclic compounds due to the reactivity of the bromo and ester groups, enabling cross-coupling reactions and nucleophilic substitutions. Its role in medicinal chemistry includes building blocks for kinase inhibitors and other bioactive molecules.
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