Ethyl 6-methyl-5-nitronicotinate

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Reagent Code: #184299
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CAS Number 1211538-09-8

science Other reagents with same CAS 1211538-09-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 210.19 g/mol
Formula C₉H₁₀N₂O₄
badge Registry Numbers
MDL Number MFCD18260802
inventory_2 Storage & Handling
Storage Room temperature, inert gas storage

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic acid derivatives with potential biological activity. It serves as a building block in the preparation of compounds studied for their use in central nervous system agents and anti-inflammatory drugs. The presence of both ester and nitro groups allows for further chemical modifications, enabling the creation of diverse heterocyclic structures important in medicinal chemistry. Commonly employed in research settings for structure-activity relationship studies in drug discovery.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿590.00
inventory 1g
10-20 days ฿790.00
inventory 5g
10-20 days ฿3,800.00
inventory 25g
10-20 days ฿17,400.00

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Ethyl 6-methyl-5-nitronicotinate
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic acid derivatives with potential biological activity. It serves as a building block in the preparation of compounds studied for their use in central nervous system agents and anti-inflammatory drugs. The presence of both ester and nitro groups allows for further chemical modifications, enabling the creation of diverse heterocyclic structures important in medicinal chemistry. Commonly employed in resea

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic acid derivatives with potential biological activity. It serves as a building block in the preparation of compounds studied for their use in central nervous system agents and anti-inflammatory drugs. The presence of both ester and nitro groups allows for further chemical modifications, enabling the creation of diverse heterocyclic structures important in medicinal chemistry. Commonly employed in research settings for structure-activity relationship studies in drug discovery.

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