Sodium 3-aminothiophene-2-carboxylate

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Reagent Code: #237017
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CAS Number 78756-27-1

science Other reagents with same CAS 78756-27-1

blur_circular Chemical Specifications

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Weight 165.15 g/mol
Formula C₅H₄NNaO₂S
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of heterocyclic compounds with biological activity. Its structure supports the formation of thiophene-based scaffolds, which are important in medicinal chemistry for designing drugs with antimicrobial, anti-inflammatory, or antitumor properties. Also employed in organic synthesis to build complex molecules through functional group transformations, taking advantage of the amine and carboxylate groups for coupling reactions.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,410.00
inventory 5g
10-20 days ฿4,890.00
inventory 10g
10-20 days ฿8,160.00
inventory 25g
10-20 days ฿17,690.00

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Sodium 3-aminothiophene-2-carboxylate
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Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of heterocyclic compounds with biological activity. Its structure supports the formation of thiophene-based scaffolds, which are important in medicinal chemistry for designing drugs with antimicrobial, anti-inflammatory, or antitumor properties. Also employed in organic synthesis to build complex molecules through functional group transformations, taking advantage of the amine and carboxylate

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of heterocyclic compounds with biological activity. Its structure supports the formation of thiophene-based scaffolds, which are important in medicinal chemistry for designing drugs with antimicrobial, anti-inflammatory, or antitumor properties. Also employed in organic synthesis to build complex molecules through functional group transformations, taking advantage of the amine and carboxylate groups for coupling reactions.

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