2-(2-Thienylcarbonyl)benzoic acid

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Reagent Code: #129618
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CAS Number 46496-80-4

science Other reagents with same CAS 46496-80-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 232.26 g/mol
Formula C₁₂H₈O₃S
badge Registry Numbers
MDL Number MFCD00101021
thermostat Physical Properties
Melting Point 143-147 °C(lit.)
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of non-steroidal anti-inflammatory drugs (NSAIDs). It serves as a key building block for thienyl-substituted compounds that exhibit anti-inflammatory and analgesic properties. Its structure allows for effective conjugation in multi-step organic reactions, making it valuable in medicinal chemistry for designing drug candidates with improved selectivity and metabolic stability. Also utilized in research settings for developing novel heterocyclic compounds with potential biological activity.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿3,730.00
inventory 5g
10-20 days ฿12,860.00

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2-(2-Thienylcarbonyl)benzoic acid
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of non-steroidal anti-inflammatory drugs (NSAIDs). It serves as a key building block for thienyl-substituted compounds that exhibit anti-inflammatory and analgesic properties. Its structure allows for effective conjugation in multi-step organic reactions, making it valuable in medicinal chemistry for designing drug candidates with improved selectivity and metabolic stability. Also utilized in research settings fo

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of non-steroidal anti-inflammatory drugs (NSAIDs). It serves as a key building block for thienyl-substituted compounds that exhibit anti-inflammatory and analgesic properties. Its structure allows for effective conjugation in multi-step organic reactions, making it valuable in medicinal chemistry for designing drug candidates with improved selectivity and metabolic stability. Also utilized in research settings for developing novel heterocyclic compounds with potential biological activity.

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