Ethyl 2-chloro-5-nitroisonicotinate

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Reagent Code: #42950
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CAS Number 907545-64-6

science Other reagents with same CAS 907545-64-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 230.61 g/mol
Formula C₈H₇ClN₂O₄
badge Registry Numbers
MDL Number MFCD22126101
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

Used primarily in organic synthesis as an intermediate for the production of agrochemicals and pharmaceuticals. It serves as a key building block in the development of herbicides and fungicides, contributing to crop protection and agricultural productivity. Additionally, it is utilized in the synthesis of active pharmaceutical ingredients (APIs) for medications targeting various diseases. Its chloro, nitro, and ester functional groups make it versatile for further chemical modifications, enabling the creation of complex molecules with specific biological activities.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿5,841.00
inventory 1g
10-20 days ฿1,827.00
inventory 10g
10-20 days ฿9,936.00

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Ethyl 2-chloro-5-nitroisonicotinate
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Used primarily in organic synthesis as an intermediate for the production of agrochemicals and pharmaceuticals. It serves as a key building block in the development of herbicides and fungicides, contributing to crop protection and agricultural productivity. Additionally, it is utilized in the synthesis of active pharmaceutical ingredients (APIs) for medications targeting various diseases. Its chloro, nitro, and ester functional groups make it versatile for further chemical modifications, enabling the cre

Used primarily in organic synthesis as an intermediate for the production of agrochemicals and pharmaceuticals. It serves as a key building block in the development of herbicides and fungicides, contributing to crop protection and agricultural productivity. Additionally, it is utilized in the synthesis of active pharmaceutical ingredients (APIs) for medications targeting various diseases. Its chloro, nitro, and ester functional groups make it versatile for further chemical modifications, enabling the creation of complex molecules with specific biological activities.

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