2-Thien-2-ylbenzoic acid

95%

Reagent Code: #132691
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CAS Number 6072-49-7

science Other reagents with same CAS 6072-49-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 204.25 g/mol
Formula C₁₁H₈O₂S
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MDL Number MFCD04039152
inventory_2 Storage & Handling
Storage Room temperature, light-proof, inert gas

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of non-steroidal anti-inflammatory drugs (NSAIDs). It serves as a building block for heterocyclic compounds due to the presence of both thiophene and carboxylic acid functional groups, enabling coupling reactions and metal-catalyzed transformations. Also employed in the preparation of organic semiconductors and conjugated polymers for electronic applications, where the thiophene moiety contributes to electron delocalization and stability. Its structure supports use in materials science for designing sensors and optoelectronic devices.

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inventory 1g
10-20 days ฿12,430.00

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2-Thien-2-ylbenzoic acid
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of non-steroidal anti-inflammatory drugs (NSAIDs). It serves as a building block for heterocyclic compounds due to the presence of both thiophene and carboxylic acid functional groups, enabling coupling reactions and metal-catalyzed transformations. Also employed in the preparation of organic semiconductors and conjugated polymers for electronic applications, where the thiophene moiety contribut

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of non-steroidal anti-inflammatory drugs (NSAIDs). It serves as a building block for heterocyclic compounds due to the presence of both thiophene and carboxylic acid functional groups, enabling coupling reactions and metal-catalyzed transformations. Also employed in the preparation of organic semiconductors and conjugated polymers for electronic applications, where the thiophene moiety contributes to electron delocalization and stability. Its structure supports use in materials science for designing sensors and optoelectronic devices.

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