Ethyl 4-chloro-2-methylnicotinate

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Reagent Code: #184909
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CAS Number 164390-30-1

science Other reagents with same CAS 164390-30-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 199.63 g/mol
Formula C₉H₁₀ClNO₂
badge Registry Numbers
MDL Number MFCD18416519
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic receptor modulators and anti-inflammatory agents. It serves as a building block in agrochemicals for the production of herbicides and plant growth regulators. Its ester and halogen functionalities allow for easy modification in organic synthesis, making it valuable in medicinal chemistry for creating diverse compound libraries. Also employed in research settings to develop new bioactive molecules due to its reactive sites and structural stability.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿4,050.00
inventory 100mg
10-20 days ฿6,750.00

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Ethyl 4-chloro-2-methylnicotinate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic receptor modulators and anti-inflammatory agents. It serves as a building block in agrochemicals for the production of herbicides and plant growth regulators. Its ester and halogen functionalities allow for easy modification in organic synthesis, making it valuable in medicinal chemistry for creating diverse compound libraries. Also employed in research settings to develop new bioactive molecules

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic receptor modulators and anti-inflammatory agents. It serves as a building block in agrochemicals for the production of herbicides and plant growth regulators. Its ester and halogen functionalities allow for easy modification in organic synthesis, making it valuable in medicinal chemistry for creating diverse compound libraries. Also employed in research settings to develop new bioactive molecules due to its reactive sites and structural stability.

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