Ethyl 2-amino-4-methylthiophene-3-carboxylate

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Reagent Code: #181823
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CAS Number 43088-42-2

science Other reagents with same CAS 43088-42-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 185.25 g/mol
Formula C₈H₁₁NO₂S
badge Registry Numbers
MDL Number MFCD00051669
thermostat Physical Properties
Melting Point 80 °C
Boiling Point 279℃
inventory_2 Storage & Handling
Density 1.219
Storage Room temperature, dry

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 heterocyclic compounds. It is also employed in the preparation of agrochemicals and dyes due to its reactive amino and ester groups. Commonly utilized in research laboratories for constructing thienopyridine and thienopyrimidine frameworks, which exhibit a range of biological activities including antimicrobial and antitumor properties.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿460.00
inventory 25g
10-20 days ฿1,860.00
inventory 100g
10-20 days ฿6,930.00
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Ethyl 2-amino-4-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 heterocyclic compounds. It is also employed in the preparation of agrochemicals and dyes due to its reactive amino and ester groups. Commonly utilized in research laboratories for constructing thienopyridine and thienopyrimidine

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 heterocyclic compounds. It is also employed in the preparation of agrochemicals and dyes due to its reactive amino and ester groups. Commonly utilized in research laboratories for constructing thienopyridine and thienopyrimidine frameworks, which exhibit a range of biological activities including antimicrobial and antitumor properties.

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