Ethyl 2-methylthiophene-3-carboxylate

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Reagent Code: #182330
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CAS Number 19432-66-7

science Other reagents with same CAS 19432-66-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 170.23 g/mol
Formula C₈H₁₀O₂S
thermostat Physical Properties
Boiling Point 222°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nonsteroidal anti-inflammatory drugs (NSAIDs) and other bioactive molecules. Its structure allows for easy functionalization, making it valuable in medicinal chemistry for building complex heterocyclic compounds. Also employed in the preparation of agrochemicals and organic semiconductors due to the electron-rich nature of the thiophene ring. Commonly utilized in research laboratories for constructing novel thienyl-based derivatives with potential biological activity.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿2,900.00
inventory 10g
10-20 days ฿25,170.00
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Ethyl 2-methylthiophene-3-carboxylate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nonsteroidal anti-inflammatory drugs (NSAIDs) and other bioactive molecules. Its structure allows for easy functionalization, making it valuable in medicinal chemistry for building complex heterocyclic compounds. Also employed in the preparation of agrochemicals and organic semiconductors due to the electron-rich nature of the thiophene ring. Commonly utilized in research laboratories for constructing novel

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nonsteroidal anti-inflammatory drugs (NSAIDs) and other bioactive molecules. Its structure allows for easy functionalization, making it valuable in medicinal chemistry for building complex heterocyclic compounds. Also employed in the preparation of agrochemicals and organic semiconductors due to the electron-rich nature of the thiophene ring. Commonly utilized in research laboratories for constructing novel thienyl-based derivatives with potential biological activity.

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