Sodium thiophene-2-carboxylate

98%

Reagent Code: #235156
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CAS Number 25112-68-9

science Other reagents with same CAS 25112-68-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 150.13 g/mol
Formula C₅H₃NaO₂S
badge Registry Numbers
MDL Number MFCD00064334
inventory_2 Storage & Handling
Storage  2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the preparation of thiophene-based active ingredients. It serves as a building block in organic reactions where the carboxylate group facilitates coupling or functionalization, enabling the development of complex heterocyclic compounds. Its sodium salt form enhances solubility and reactivity in polar solvents, making it suitable for catalytic transformations and cross-coupling reactions. Also employed in materials science for designing conductive polymers and organic semiconductors due to the electron-rich nature of the thiophene ring.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿620.00
inventory 100g
10-20 days ฿7,810.00
inventory 500g
10-20 days ฿26,470.00
inventory 25g
10-20 days ฿2,480.00
Sodium thiophene-2-carboxylate
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Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the preparation of thiophene-based active ingredients. It serves as a building block in organic reactions where the carboxylate group facilitates coupling or functionalization, enabling the development of complex heterocyclic compounds. Its sodium salt form enhances solubility and reactivity in polar solvents, making it suitable for catalytic transformations and cross-coupling reactions. Also employed in mat

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the preparation of thiophene-based active ingredients. It serves as a building block in organic reactions where the carboxylate group facilitates coupling or functionalization, enabling the development of complex heterocyclic compounds. Its sodium salt form enhances solubility and reactivity in polar solvents, making it suitable for catalytic transformations and cross-coupling reactions. Also employed in materials science for designing conductive polymers and organic semiconductors due to the electron-rich nature of the thiophene ring.

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