Ethyl 2-formylthiophene-3-carboxylate

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Reagent Code: #182821
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CAS Number 67808-70-2

science Other reagents with same CAS 67808-70-2

blur_circular Chemical Specifications

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Weight 184.21 g/mol
Formula C₈H₈O₃S
inventory_2 Storage & Handling
Storage 2-8°C, inert gas atmosphere

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of biologically active heterocyclic compounds. Its aldehyde and ester functional groups allow for versatile chemical transformations, such as condensation and cyclization reactions, making it valuable in constructing complex thiophene-based structures. Commonly employed in the preparation of dyes, fluorescent probes, and organic semiconductors due to the electron-rich nature of the thiophene ring. Also utilized in research settings for the development of novel materials and drug candidates.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿1,470.00
inventory 250mg
10-20 days ฿4,950.00
inventory 1g
10-20 days ฿13,960.00
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Ethyl 2-formylthiophene-3-carboxylate
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Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of biologically active heterocyclic compounds. Its aldehyde and ester functional groups allow for versatile chemical transformations, such as condensation and cyclization reactions, making it valuable in constructing complex thiophene-based structures. Commonly employed in the preparation of dyes, fluorescent probes, and organic semiconductors due to the electron-rich nature of the thiophene

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of biologically active heterocyclic compounds. Its aldehyde and ester functional groups allow for versatile chemical transformations, such as condensation and cyclization reactions, making it valuable in constructing complex thiophene-based structures. Commonly employed in the preparation of dyes, fluorescent probes, and organic semiconductors due to the electron-rich nature of the thiophene ring. Also utilized in research settings for the development of novel materials and drug candidates.

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