5-Acetylthiophene-2-carboxylic Acid

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Reagent Code: #136162
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CAS Number 4066-41-5

science Other reagents with same CAS 4066-41-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 170.18 g/mol
Formula C₇H₆O₃S
badge Registry Numbers
MDL Number MFCD00055512
thermostat Physical Properties
Melting Point 211°C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of antidiabetic and anti-inflammatory agents. Its structure supports the formation of heterocyclic compounds that are key in drug design. The presence of carboxylic acid and acetyl groups on the thiophene ring facilitates further reactions, such as amide formation with amines or reduction of the carbonyl to alcohols. Also employed in the preparation of organic semiconductors due to the thiophene ring, which enhances electronic properties in conjugated systems. Additionally, it serves as a building block in agrochemicals for creating active ingredients in crop protection products.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿900.00
inventory 25g
10-20 days ฿4,290.00
inventory 100g
10-20 days ฿16,020.00

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5-Acetylthiophene-2-carboxylic Acid
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of antidiabetic and anti-inflammatory agents. Its structure supports the formation of heterocyclic compounds that are key in drug design. The presence of carboxylic acid and acetyl groups on the thiophene ring facilitates further reactions, such as amide formation with amines or reduction of the carbonyl to alcohols. Also employed in the preparation of organic semiconductors due to the thiophene ring, which enhan

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of antidiabetic and anti-inflammatory agents. Its structure supports the formation of heterocyclic compounds that are key in drug design. The presence of carboxylic acid and acetyl groups on the thiophene ring facilitates further reactions, such as amide formation with amines or reduction of the carbonyl to alcohols. Also employed in the preparation of organic semiconductors due to the thiophene ring, which enhances electronic properties in conjugated systems. Additionally, it serves as a building block in agrochemicals for creating active ingredients in crop protection products.

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