Ethyl 5-chloro-4-nitrothiophene-2-carboxylate

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Reagent Code: #182651
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CAS Number 89640-03-9

science Other reagents with same CAS 89640-03-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 235.65 g/mol
Formula C₇H₆ClNO₄S
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules due to the presence of reactive functional groups. The nitro and chloro substituents allow for sequential substitution reactions, enabling the introduction of various nucleophiles. Commonly employed in heterocyclic chemistry to construct complex thiophene-based compounds with potential antimicrobial, antifungal, or anti-inflammatory properties. Also utilized in material science for designing organic semiconductors and conjugated polymers, where the thiophene core contributes to electron-rich character and stability.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿570.00
inventory 1g
10-20 days ฿1,040.00
inventory 5g
10-20 days ฿4,720.00
inventory 10g
10-20 days ฿8,550.00
inventory 25g
10-20 days ฿16,460.00
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Ethyl 5-chloro-4-nitrothiophene-2-carboxylate
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules due to the presence of reactive functional groups. The nitro and chloro substituents allow for sequential substitution reactions, enabling the introduction of various nucleophiles. Commonly employed in heterocyclic chemistry to construct complex thiophene-based compounds with potential antimicrobial, antifungal, or anti-inflammatory properties. Also utilized in material sc

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules due to the presence of reactive functional groups. The nitro and chloro substituents allow for sequential substitution reactions, enabling the introduction of various nucleophiles. Commonly employed in heterocyclic chemistry to construct complex thiophene-based compounds with potential antimicrobial, antifungal, or anti-inflammatory properties. Also utilized in material science for designing organic semiconductors and conjugated polymers, where the thiophene core contributes to electron-rich character and stability.

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